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6505-01-492-5820

20 Products

NDC58160-0856-56

HEPATITIS B VIRUS VACCINE,INACTIVATED,MODIFIED

NSN, MFG P/N

6505014925820

NSN

6505-01-492-5820

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NDC58160-0856-56

HEPATITIS B VIRUS VACCINE,INACTIVATED,MODIFIED

NSN, MFG P/N

6505014925820

NSN

6505-01-492-5820

MFG

GLAXO WELLCOME INC

Description

III PART NAME ASSIGNED BY CONTROLLING AGENCY: HEPATITIS B VIRUS VACCINE INACTIVATED 10MCG/0.5ML SYRINGE 25S
III PROTECTIVE STORAGE FEATURE: REQUIRES REFRIGERATION BETWEEN 2 DEG TO 8 DEG C
III SUPPLEMENTARY FEATURES: SINGLE-DOSE PRE-FILLED DISPOSABLE TIP-LOK SYRINGES WITH 1-INCH 23-GAUGE NEEDLES
IMMEDIATE CONTAINER TYPE: SYRINGE-NEEDLE UNIT
SPECIAL FEATURES: RECOMBINANT; PEDIATRIC/ADOLESCENT; EACH 0.5 ML OF VACCINE CONSISTS OF 10 MCG OF HEPATITIS B SURFACE ANTIGEN ADSORBED ON 0.25 MG ALUMINUM AS ALUMINUM HYDROXIDE; IS FORMULATED WITHOUT PERSERVATIVES; SUPPLIED AS A STERILE SUSPENSION FOR INTRAMUSCULAR
UNIT PACKAGE QUANTITY: 25
UNIT PACKAGE TYPE: PACKAGE
~1: ADMINISTRATION; READY FOR USE WITHOUT RECONSTITUTION. DO NOT FREEZE, DICARD IF PRODUCT HAS BEEN FROZEN. DO NOT DILUTE TO ADMINISTER

ENGERIX-B

HEPATITIS B VIRUS VACCINE,INACTIVATED,MODIFIED

NSN, MFG P/N

6505014925820

NSN

6505-01-492-5820

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ENGERIX-B

HEPATITIS B VIRUS VACCINE,INACTIVATED,MODIFIED

NSN, MFG P/N

6505014925820

NSN

6505-01-492-5820

MFG

GLAXO WELLCOME INC

Description

III PART NAME ASSIGNED BY CONTROLLING AGENCY: HEPATITIS B VIRUS VACCINE INACTIVATED 10MCG/0.5ML SYRINGE 25S
III PROTECTIVE STORAGE FEATURE: REQUIRES REFRIGERATION BETWEEN 2 DEG TO 8 DEG C
III SUPPLEMENTARY FEATURES: SINGLE-DOSE PRE-FILLED DISPOSABLE TIP-LOK SYRINGES WITH 1-INCH 23-GAUGE NEEDLES
IMMEDIATE CONTAINER TYPE: SYRINGE-NEEDLE UNIT
SPECIAL FEATURES: RECOMBINANT; PEDIATRIC/ADOLESCENT; EACH 0.5 ML OF VACCINE CONSISTS OF 10 MCG OF HEPATITIS B SURFACE ANTIGEN ADSORBED ON 0.25 MG ALUMINUM AS ALUMINUM HYDROXIDE; IS FORMULATED WITHOUT PERSERVATIVES; SUPPLIED AS A STERILE SUSPENSION FOR INTRAMUSCULAR
UNIT PACKAGE QUANTITY: 25
UNIT PACKAGE TYPE: PACKAGE
~1: ADMINISTRATION; READY FOR USE WITHOUT RECONSTITUTION. DO NOT FREEZE, DICARD IF PRODUCT HAS BEEN FROZEN. DO NOT DILUTE TO ADMINISTER

ENGERIX-B

HEPATITIS B VIRUS VACCINE,INACTIVATED,MODIFIED

NSN, MFG P/N

6505014925821

NSN

6505-01-492-5821

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ENGERIX-B

HEPATITIS B VIRUS VACCINE,INACTIVATED,MODIFIED

NSN, MFG P/N

6505014925821

NSN

6505-01-492-5821

MFG

GLAXO WELLCOME INC

Description

III PART NAME ASSIGNED BY CONTROLLING AGENCY: HEPATITIS B VIRUS VACCINE INACTIVATED 10MCG/0.25MG VIAL 10S
III PROTECTIVE STORAGE FEATURE: REQUIRES REFRIGERATION BETWEEN 2 DEG TO 8 DEG C
IMMEDIATE CONTAINER TYPE: VIAL
SPECIAL FEATURES: RECOMBINANT; PEDIATRIC/ADOLESCENT; EACH 0.5 ML OF VACCINE CONSISTS OF 10 MCG OF HEPATITIS B SURFACE ANTIGEN ADSORBED ON 0.25 MG ALUMINUM AS ALUMINUM HYDROXIDE.THE VACCINE IS FORMULATED WITHOUT PRESERVATIVES; IS SUPPLIED AS A STERILE SUSPENSION FOR
UNIT PACKAGE QUANTITY: 10
UNIT PACKAGE TYPE: PACKAGE
~1: INTRAMUSCULAR ADMINISTRATION,IS READY FOR USE WITHOUT RECONSTITUTION. DO NOT FREEZE, DISCARD IF PRODUCT HAS BEEN FROZEN. DO NOT DILUTE TO ADMINISTER

NDC58160-0820-11

HEPATITIS B VIRUS VACCINE,INACTIVATED,MODIFIED

NSN, MFG P/N

6505014925821

NSN

6505-01-492-5821

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NDC58160-0820-11

HEPATITIS B VIRUS VACCINE,INACTIVATED,MODIFIED

NSN, MFG P/N

6505014925821

NSN

6505-01-492-5821

MFG

GLAXO WELLCOME INC

Description

III PART NAME ASSIGNED BY CONTROLLING AGENCY: HEPATITIS B VIRUS VACCINE INACTIVATED 10MCG/0.25MG VIAL 10S
III PROTECTIVE STORAGE FEATURE: REQUIRES REFRIGERATION BETWEEN 2 DEG TO 8 DEG C
IMMEDIATE CONTAINER TYPE: VIAL
SPECIAL FEATURES: RECOMBINANT; PEDIATRIC/ADOLESCENT; EACH 0.5 ML OF VACCINE CONSISTS OF 10 MCG OF HEPATITIS B SURFACE ANTIGEN ADSORBED ON 0.25 MG ALUMINUM AS ALUMINUM HYDROXIDE.THE VACCINE IS FORMULATED WITHOUT PRESERVATIVES; IS SUPPLIED AS A STERILE SUSPENSION FOR
UNIT PACKAGE QUANTITY: 10
UNIT PACKAGE TYPE: PACKAGE
~1: INTRAMUSCULAR ADMINISTRATION,IS READY FOR USE WITHOUT RECONSTITUTION. DO NOT FREEZE, DISCARD IF PRODUCT HAS BEEN FROZEN. DO NOT DILUTE TO ADMINISTER

04-0878

METHYLPREDNISOLONE SODIUM SUCCINATE FOR INJECTION,USP

NSN, MFG P/N

6505014925896

NSN

6505-01-492-5896

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04-0878

METHYLPREDNISOLONE SODIUM SUCCINATE FOR INJECTION,USP

NSN, MFG P/N

6505014925896

NSN

6505-01-492-5896

MFG

DEFENSE LOGISTICS AGENCY DIRECTORATE OF MEDICAL MATERIEL DEFENSE SUPPLY CENTER PHILADELPHIA

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 125.000 MILLIGRAMS METHYLPREDNISOLONE ACTIVE INGREDIENT
FEATURES PROVIDED: DILUENT AND STERILE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: METHYLPREDNISOLONE SODIUM SUCCINATE FOR INJECTION USP 125MG POWDER VIAL 25S
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 2.000 MILLILITERS AFTER RECONSTITUTION
PRIMARY CONTAINER TYPE: VIAL
TOTAL PRIMARY CONTAINER QUANTITY: 25

NDC00009-0190-16

METHYLPREDNISOLONE SODIUM SUCCINATE FOR INJECTION,USP

NSN, MFG P/N

6505014925896

NSN

6505-01-492-5896

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NDC00009-0190-16

METHYLPREDNISOLONE SODIUM SUCCINATE FOR INJECTION,USP

NSN, MFG P/N

6505014925896

NSN

6505-01-492-5896

MFG

VETERANS HEALTH

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 125.000 MILLIGRAMS METHYLPREDNISOLONE ACTIVE INGREDIENT
FEATURES PROVIDED: DILUENT AND STERILE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: METHYLPREDNISOLONE SODIUM SUCCINATE FOR INJECTION USP 125MG POWDER VIAL 25S
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 2.000 MILLILITERS AFTER RECONSTITUTION
PRIMARY CONTAINER TYPE: VIAL
TOTAL PRIMARY CONTAINER QUANTITY: 25

SOLU-MEDROL

METHYLPREDNISOLONE SODIUM SUCCINATE FOR INJECTION,USP

NSN, MFG P/N

6505014925896

NSN

6505-01-492-5896

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SOLU-MEDROL

METHYLPREDNISOLONE SODIUM SUCCINATE FOR INJECTION,USP

NSN, MFG P/N

6505014925896

NSN

6505-01-492-5896

MFG

PHARMACIA & UPJOHN COMPANY

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 125.000 MILLIGRAMS METHYLPREDNISOLONE ACTIVE INGREDIENT
FEATURES PROVIDED: DILUENT AND STERILE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: METHYLPREDNISOLONE SODIUM SUCCINATE FOR INJECTION USP 125MG POWDER VIAL 25S
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 2.000 MILLILITERS AFTER RECONSTITUTION
PRIMARY CONTAINER TYPE: VIAL
TOTAL PRIMARY CONTAINER QUANTITY: 25

01-0652

DEXAMETHASONE SODIUM PHOSPHATE INJECTION,USP

NSN, MFG P/N

6505014926420

NSN

6505-01-492-6420

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01-0652

DEXAMETHASONE SODIUM PHOSPHATE INJECTION,USP

NSN, MFG P/N

6505014926420

NSN

6505-01-492-6420

MFG

DEFENSE LOGISTICS AGENCY DIRECTORATE OF MEDICAL MATERIEL DEFENSE SUPPLY CENTER PHILADELPHIA

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 4.000 MILLIGRAMS DEXAMETHASONE SODIUM PHOSPHATE PER MILLILITER
ADMINISTRATION: INTRAVENOUS OR INTRAMUSCULAR OR INTRA-ARTICULAR OR INTRALESIONAL OR SOFT TISSUE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: DEXAMETHASONE INJ 4MG/ML, 5ML VIAL, 25 VIAL/PACKAGE
PRIMARY CONTAINER CONTENT QUANTITY: 5.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL, SINGLE DOSE
SECONDARY CONTAINER TYPE: BOX
SPECIAL FEATURES: STORE AT CONTROLLED ROOM TEMP 15 TO 30 DEG C; SENSITIVE TO HEAT, DO NOT AUTOCLAVE USE PREFERRED JDF NSN 6505015225164
TOTAL PRIMARY CONTAINER QUANTITY: 25

NDC00517-4905-25

DEXAMETHASONE SODIUM PHOSPHATE INJECTION,USP

NSN, MFG P/N

6505014926420

NSN

6505-01-492-6420

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NDC00517-4905-25

DEXAMETHASONE SODIUM PHOSPHATE INJECTION,USP

NSN, MFG P/N

6505014926420

NSN

6505-01-492-6420

MFG

LUITPOLD PHARMACEUTICALS INC OSTEOHEALTH COMPANY OSTEOHEALTH DIV

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 4.000 MILLIGRAMS DEXAMETHASONE SODIUM PHOSPHATE PER MILLILITER
ADMINISTRATION: INTRAVENOUS OR INTRAMUSCULAR OR INTRA-ARTICULAR OR INTRALESIONAL OR SOFT TISSUE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: DEXAMETHASONE INJ 4MG/ML, 5ML VIAL, 25 VIAL/PACKAGE
PRIMARY CONTAINER CONTENT QUANTITY: 5.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL, SINGLE DOSE
SECONDARY CONTAINER TYPE: BOX
SPECIAL FEATURES: STORE AT CONTROLLED ROOM TEMP 15 TO 30 DEG C; SENSITIVE TO HEAT, DO NOT AUTOCLAVE USE PREFERRED JDF NSN 6505015225164
TOTAL PRIMARY CONTAINER QUANTITY: 25

01-0683

DOXYCYCLINE MONOHYDRATE FOR ORAL SUSPENSION

NSN, MFG P/N

6505014926461

NSN

6505-01-492-6461

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01-0683

DOXYCYCLINE MONOHYDRATE FOR ORAL SUSPENSION

NSN, MFG P/N

6505014926461

NSN

6505-01-492-6461

MFG

DEFENSE LOGISTICS AGENCY DIRECTORATE OF MEDICAL MATERIEL DEFENSE SUPPLY CENTER PHILADELPHIA

Description

ADMINISTRATION: ORAL
FLAVOR: RASPBERRY
III PART NAME ASSIGNED BY CONTROLLING AGENCY: DOXYCYCLINE MONOHYDRATE FOR ORAL SUSPENSION 25MG PER 60ML POWDER BT
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 20.500 GRAMS
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: 25 MG OF DOXYCYCLINE PER 5 ML; CONTAINS 60 ML AFTER RECONSTITUTION OF DRY POWDER FOR ORAL SUSPENSION; PEDIATRIC; STORE BELOW 86 DEG F; DISPENSED IN TIGHT, LIGHT RESISTANT CONTAINERS

NDC00069-0970-65

DOXYCYCLINE MONOHYDRATE FOR ORAL SUSPENSION

NSN, MFG P/N

6505014926461

NSN

6505-01-492-6461

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NDC00069-0970-65

DOXYCYCLINE MONOHYDRATE FOR ORAL SUSPENSION

NSN, MFG P/N

6505014926461

NSN

6505-01-492-6461

MFG

PFIZER INC. DBA PFIZER

Description

ADMINISTRATION: ORAL
FLAVOR: RASPBERRY
III PART NAME ASSIGNED BY CONTROLLING AGENCY: DOXYCYCLINE MONOHYDRATE FOR ORAL SUSPENSION 25MG PER 60ML POWDER BT
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 20.500 GRAMS
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: 25 MG OF DOXYCYCLINE PER 5 ML; CONTAINS 60 ML AFTER RECONSTITUTION OF DRY POWDER FOR ORAL SUSPENSION; PEDIATRIC; STORE BELOW 86 DEG F; DISPENSED IN TIGHT, LIGHT RESISTANT CONTAINERS

VIBRAMYCIN

DOXYCYCLINE MONOHYDRATE FOR ORAL SUSPENSION

NSN, MFG P/N

6505014926461

NSN

6505-01-492-6461

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VIBRAMYCIN

DOXYCYCLINE MONOHYDRATE FOR ORAL SUSPENSION

NSN, MFG P/N

6505014926461

NSN

6505-01-492-6461

MFG

PFIZER INC. DBA PFIZER

Description

ADMINISTRATION: ORAL
FLAVOR: RASPBERRY
III PART NAME ASSIGNED BY CONTROLLING AGENCY: DOXYCYCLINE MONOHYDRATE FOR ORAL SUSPENSION 25MG PER 60ML POWDER BT
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 20.500 GRAMS
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: 25 MG OF DOXYCYCLINE PER 5 ML; CONTAINS 60 ML AFTER RECONSTITUTION OF DRY POWDER FOR ORAL SUSPENSION; PEDIATRIC; STORE BELOW 86 DEG F; DISPENSED IN TIGHT, LIGHT RESISTANT CONTAINERS

01-0656

HAEMOPHILUS B POLYSACCHARIDE CONJUGATE (DIPHTHERIA TOXOID CONJUGATE) VACCINE

NSN, MFG P/N

6505014926474

NSN

6505-01-492-6474

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01-0656

HAEMOPHILUS B POLYSACCHARIDE CONJUGATE (DIPHTHERIA TOXOID CONJUGATE) VACCINE

NSN, MFG P/N

6505014926474

NSN

6505-01-492-6474

MFG

DEFENSE LOGISTICS AGENCY DIRECTORATE OF MEDICAL MATERIEL DEFENSE SUPPLY CENTER PHILADELPHIA

Description

III PART NAME ASSIGNED BY CONTROLLING AGENCY: HAEMOPHILUS B POLYSACCHARIDE CONJUGATE VACCINE 0.6ML/DILUENT VIAL 5S
IMMEDIATE CONTAINER QUANTITY: 5
IMMEDIATE CONTAINER TYPE: VIAL
QUANTITY WITHIN EACH IMMEDIATE CONTAINER: 1 SINGLE DOSE WITH 0.6 ML VIAL CONTAINING DILUENT
SPECIAL FEATURES: STERILE, LYOPHILIZED POWDER RECONSTITUTED AT TIME OF USE WITH EITHER SALINE DILUENT (0.4% SODIUM CHLORIDE) OR AVENTIS PASTEUR INC DIPHTHERIA AND TETANUS TOXOIDS AND PERTUSSIS VACCINE ADSORBED FOR INTRAMUSCULAR USE ONLY CONTAINS NO PRESERVATIVE; CONSISTS
UNIT PACKAGE TYPE: PACKAGE
~1: OF THE HAEMOPHILUS B CAPSULAR POLYSACCHARIDE PREPARED FROM THE H. INFLUENZAE TYPE B STRAIN 1482 AND COVALENTLY BOUND TO TETANUS TOXOID

ACTHIB W/0.4% NACL DILUENT

HAEMOPHILUS B POLYSACCHARIDE CONJUGATE (DIPHTHERIA TOXOID CONJUGATE) VACCINE

NSN, MFG P/N

6505014926474

NSN

6505-01-492-6474

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ACTHIB W/0.4% NACL DILUENT

HAEMOPHILUS B POLYSACCHARIDE CONJUGATE (DIPHTHERIA TOXOID CONJUGATE) VACCINE

NSN, MFG P/N

6505014926474

NSN

6505-01-492-6474

MFG

SANOFI PASTEUR INC.

Description

III PART NAME ASSIGNED BY CONTROLLING AGENCY: HAEMOPHILUS B POLYSACCHARIDE CONJUGATE VACCINE 0.6ML/DILUENT VIAL 5S
IMMEDIATE CONTAINER QUANTITY: 5
IMMEDIATE CONTAINER TYPE: VIAL
QUANTITY WITHIN EACH IMMEDIATE CONTAINER: 1 SINGLE DOSE WITH 0.6 ML VIAL CONTAINING DILUENT
SPECIAL FEATURES: STERILE, LYOPHILIZED POWDER RECONSTITUTED AT TIME OF USE WITH EITHER SALINE DILUENT (0.4% SODIUM CHLORIDE) OR AVENTIS PASTEUR INC DIPHTHERIA AND TETANUS TOXOIDS AND PERTUSSIS VACCINE ADSORBED FOR INTRAMUSCULAR USE ONLY CONTAINS NO PRESERVATIVE; CONSISTS
UNIT PACKAGE TYPE: PACKAGE
~1: OF THE HAEMOPHILUS B CAPSULAR POLYSACCHARIDE PREPARED FROM THE H. INFLUENZAE TYPE B STRAIN 1482 AND COVALENTLY BOUND TO TETANUS TOXOID

NDC49281-0545-05

HAEMOPHILUS B POLYSACCHARIDE CONJUGATE (DIPHTHERIA TOXOID CONJUGATE) VACCINE

NSN, MFG P/N

6505014926474

NSN

6505-01-492-6474

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NDC49281-0545-05

HAEMOPHILUS B POLYSACCHARIDE CONJUGATE (DIPHTHERIA TOXOID CONJUGATE) VACCINE

NSN, MFG P/N

6505014926474

NSN

6505-01-492-6474

MFG

CARDINAL HEALTH INC. DBA CARDINAL HEALTH

Description

III PART NAME ASSIGNED BY CONTROLLING AGENCY: HAEMOPHILUS B POLYSACCHARIDE CONJUGATE VACCINE 0.6ML/DILUENT VIAL 5S
IMMEDIATE CONTAINER QUANTITY: 5
IMMEDIATE CONTAINER TYPE: VIAL
QUANTITY WITHIN EACH IMMEDIATE CONTAINER: 1 SINGLE DOSE WITH 0.6 ML VIAL CONTAINING DILUENT
SPECIAL FEATURES: STERILE, LYOPHILIZED POWDER RECONSTITUTED AT TIME OF USE WITH EITHER SALINE DILUENT (0.4% SODIUM CHLORIDE) OR AVENTIS PASTEUR INC DIPHTHERIA AND TETANUS TOXOIDS AND PERTUSSIS VACCINE ADSORBED FOR INTRAMUSCULAR USE ONLY CONTAINS NO PRESERVATIVE; CONSISTS
UNIT PACKAGE TYPE: PACKAGE
~1: OF THE HAEMOPHILUS B CAPSULAR POLYSACCHARIDE PREPARED FROM THE H. INFLUENZAE TYPE B STRAIN 1482 AND COVALENTLY BOUND TO TETANUS TOXOID

01-0692

HEPATITIS B VIRUS VACCINE,INACTIVATED,MODIFIED

NSN, MFG P/N

6505014926608

NSN

6505-01-492-6608

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01-0692

HEPATITIS B VIRUS VACCINE,INACTIVATED,MODIFIED

NSN, MFG P/N

6505014926608

NSN

6505-01-492-6608

MFG

DEFENSE LOGISTICS AGENCY DIRECTORATE OF MEDICAL MATERIEL DEFENSE SUPPLY CENTER PHILADELPHIA

Description

III PART NAME ASSIGNED BY CONTROLLING AGENCY: HEPATITIS B VIRUS VACCINE INACTIVATED 10MCG/0.5ML SYRINGE 25S
III PROTECTIVE STORAGE FEATURE: REQUIRES REFRIGERATION BETWEEN 2 DEG TO 8 DEG C
III SUPPLEMENTARY FEATURES: SINGLE-DOSE PREFILLED DISPOSABLE TIP-LOK SYRINGES WITH 5/8-INCH 25-GAUGE SAFETYGLIDE NEEDLES
IMMEDIATE CONTAINER TYPE: SYRINGE-NEEDLE UNIT
SPECIAL FEATURES: RECOMBINANT; PEDIATRIC/ADOLESCENT; EACH 0.5 ML OF VACCINE CONSISTS OF 10 MCG OF HEPATITIS B SURFACE ANTIGEN ADSORBED ON 0.25 MG ALUMINUM AS ALUMINUM HYDROXIDE; IS FORMULATED WITHOUT PERSERVATIVES; SUPPLIED AS A STERILE SUSPENSION FOR INTRAMUSCULAR
UNIT PACKAGE QUANTITY: 25
UNIT PACKAGE TYPE: PACKAGE
~1: ADMINISTRATION; READY FOR USE WITHOUT RECONSTITUTION. DO NOT FREEZE, DISCARD IF PRODUCT HAS BEEN FROZEN. DO NOT DILUTE TO ADMINISTER

ENGERIX-B

HEPATITIS B VIRUS VACCINE,INACTIVATED,MODIFIED

NSN, MFG P/N

6505014926608

NSN

6505-01-492-6608

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ENGERIX-B

HEPATITIS B VIRUS VACCINE,INACTIVATED,MODIFIED

NSN, MFG P/N

6505014926608

NSN

6505-01-492-6608

MFG

SMITH KLINE BEECHMAN PHARMACEUTICALS

Description

III PART NAME ASSIGNED BY CONTROLLING AGENCY: HEPATITIS B VIRUS VACCINE INACTIVATED 10MCG/0.5ML SYRINGE 25S
III PROTECTIVE STORAGE FEATURE: REQUIRES REFRIGERATION BETWEEN 2 DEG TO 8 DEG C
III SUPPLEMENTARY FEATURES: SINGLE-DOSE PREFILLED DISPOSABLE TIP-LOK SYRINGES WITH 5/8-INCH 25-GAUGE SAFETYGLIDE NEEDLES
IMMEDIATE CONTAINER TYPE: SYRINGE-NEEDLE UNIT
SPECIAL FEATURES: RECOMBINANT; PEDIATRIC/ADOLESCENT; EACH 0.5 ML OF VACCINE CONSISTS OF 10 MCG OF HEPATITIS B SURFACE ANTIGEN ADSORBED ON 0.25 MG ALUMINUM AS ALUMINUM HYDROXIDE; IS FORMULATED WITHOUT PERSERVATIVES; SUPPLIED AS A STERILE SUSPENSION FOR INTRAMUSCULAR
UNIT PACKAGE QUANTITY: 25
UNIT PACKAGE TYPE: PACKAGE
~1: ADMINISTRATION; READY FOR USE WITHOUT RECONSTITUTION. DO NOT FREEZE, DISCARD IF PRODUCT HAS BEEN FROZEN. DO NOT DILUTE TO ADMINISTER

NDC58160-0856-57

HEPATITIS B VIRUS VACCINE,INACTIVATED,MODIFIED

NSN, MFG P/N

6505014926608

NSN

6505-01-492-6608

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NDC58160-0856-57

HEPATITIS B VIRUS VACCINE,INACTIVATED,MODIFIED

NSN, MFG P/N

6505014926608

NSN

6505-01-492-6608

MFG

SMITH KLINE BEECHMAN PHARMACEUTICALS

Description

III PART NAME ASSIGNED BY CONTROLLING AGENCY: HEPATITIS B VIRUS VACCINE INACTIVATED 10MCG/0.5ML SYRINGE 25S
III PROTECTIVE STORAGE FEATURE: REQUIRES REFRIGERATION BETWEEN 2 DEG TO 8 DEG C
III SUPPLEMENTARY FEATURES: SINGLE-DOSE PREFILLED DISPOSABLE TIP-LOK SYRINGES WITH 5/8-INCH 25-GAUGE SAFETYGLIDE NEEDLES
IMMEDIATE CONTAINER TYPE: SYRINGE-NEEDLE UNIT
SPECIAL FEATURES: RECOMBINANT; PEDIATRIC/ADOLESCENT; EACH 0.5 ML OF VACCINE CONSISTS OF 10 MCG OF HEPATITIS B SURFACE ANTIGEN ADSORBED ON 0.25 MG ALUMINUM AS ALUMINUM HYDROXIDE; IS FORMULATED WITHOUT PERSERVATIVES; SUPPLIED AS A STERILE SUSPENSION FOR INTRAMUSCULAR
UNIT PACKAGE QUANTITY: 25
UNIT PACKAGE TYPE: PACKAGE
~1: ADMINISTRATION; READY FOR USE WITHOUT RECONSTITUTION. DO NOT FREEZE, DISCARD IF PRODUCT HAS BEEN FROZEN. DO NOT DILUTE TO ADMINISTER

ICT MALARIA TEST

MALARIA TEST

NSN, MFG P/N

6505014926996

NSN

6505-01-492-6996

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ICT MALARIA TEST

MALARIA TEST

NSN, MFG P/N

6505014926996

NSN

6505-01-492-6996

MFG

BINAX INC DBA INVERNESS MEDICAL PROFESSIONAL DIAGNOSTICS

01-0682

CIPROFLOXACIN ORAL

NSN, MFG P/N

6505014928089

NSN

6505-01-492-8089

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01-0682

CIPROFLOXACIN ORAL

NSN, MFG P/N

6505014928089

NSN

6505-01-492-8089

MFG

DEFENSE LOGISTICS AGENCY DIRECTORATE OF MEDICAL MATERIEL DEFENSE SUPPLY CENTER PHILADELPHIA

Description

III PART NAME ASSIGNED BY CONTROLLING AGENCY: CIPROFLOXACIN SUSPENSION 250MG/5ML 100ML AFTER RECONSTITUTION
SPECIAL FEATURES: CIPROFLOXACIN MICROENCAPSULATED; 250 MG PER 5 ML, 100 ML AFTER RECONSTITUTION, ORAL SUSPENSION; THE DRUG IS COMPOSED OF TWO COMPONENTS (MICROCAPSULES AND DILUENT); STORE BELOW 25 DEGREES C (77 DEGREES F) PROTECT FROM FREEZING