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6505-01-284-5150

20 Products

NDC00172-2982-60

CHLORDIAZEPOXIDE HYDROCHLORIDE AND CLIDINIUM BROMIDE CAPSULES

NSN, MFG P/N

6505012845150

NSN

6505-01-284-5150

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NDC00172-2982-60

CHLORDIAZEPOXIDE HYDROCHLORIDE AND CLIDINIUM BROMIDE CAPSULES

NSN, MFG P/N

6505012845150

NSN

6505-01-284-5150

MFG

ZENITH LABORATORIES INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 5.000 MILLIGRAMS CHLORDIAZEPOXIDE HYDROCHLORIDE ACTIVE INGREDIENT AND 2.500 MILLIGRAMS CLIDINIUM BROMIDE ACTIVE INGREDIENT
ADMINISTRATION: ORAL
CAPSULE CONTENT FORM: ANY ACCEPTABLE
CAPSULE PRIMARY CONTAINER CONTENT QUANTITY: 100.000
CAPSULE TYPE: ANY ACCEPTABLE
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: ACTIVE MEDICAMENT MEDICINAL STRENGTH:5.000 MILLIGRAMS OF CHLORDIAZEPOXIDE ACTIVE INGREDIENTS

NDC18393-0272-02

NAPROXEN TABLETS,USP

NSN, MFG P/N

6505012840271

NSN

6505-01-284-0271

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NDC18393-0272-02

NAPROXEN TABLETS,USP

NSN, MFG P/N

6505012840271

NSN

6505-01-284-0271

MFG

SYNTEX LABORATORIES INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 250.000 MILLIGRAMS NAPROXEN ACTIVE INGREDIENT
PRIMARY CONTAINER CONTENT QUANTITY: 60.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: UNIT OF USE

1192

LIDOCAINE HYDROCHLORIDE INJECTION,USP

NSN, MFG P/N

6505012840272

NSN

6505-01-284-0272

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1192

LIDOCAINE HYDROCHLORIDE INJECTION,USP

NSN, MFG P/N

6505012840272

NSN

6505-01-284-0272

MFG

INTERNATIONAL MEDICATION SYSTEMS LTD.

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 1.000 PERCENTAGE, W/V LIDOCAINE HYDROCHLORIDE ACTIVE INGREDIENT
ADMINISTRATION: INTRACARDIAL
FEATURES PROVIDED: STERILE
PRIMARY CONTAINER CONTENT QUANTITY: 5.000 MILLILITERS
PRIMARY CONTAINER TYPE: SYRINGE WITH NEEDLE
SPECIAL FEATURES: EACH SYRINGE CONTAINS 50 MG. LIDOCAINE HYDROCHLORIDE; NEEDLE SIZE 21 GAGE BY 1-1/2 INCHES; WITHOUT EPINEPHARINE
TOTAL PRIMARY CONTAINER QUANTITY: 10

NDC00548-1192-00

LIDOCAINE HYDROCHLORIDE INJECTION,USP

NSN, MFG P/N

6505012840272

NSN

6505-01-284-0272

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NDC00548-1192-00

LIDOCAINE HYDROCHLORIDE INJECTION,USP

NSN, MFG P/N

6505012840272

NSN

6505-01-284-0272

MFG

INTERNATIONAL MEDICATION SYSTEMS LTD.

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 1.000 PERCENTAGE, W/V LIDOCAINE HYDROCHLORIDE ACTIVE INGREDIENT
ADMINISTRATION: INTRACARDIAL
FEATURES PROVIDED: STERILE
PRIMARY CONTAINER CONTENT QUANTITY: 5.000 MILLILITERS
PRIMARY CONTAINER TYPE: SYRINGE WITH NEEDLE
SPECIAL FEATURES: EACH SYRINGE CONTAINS 50 MG. LIDOCAINE HYDROCHLORIDE; NEEDLE SIZE 21 GAGE BY 1-1/2 INCHES; WITHOUT EPINEPHARINE
TOTAL PRIMARY CONTAINER QUANTITY: 10

NDC00486-1125-05

POTASSIUM PHOSPHATE,MONOBASIC,TABLETS

NSN, MFG P/N

6505012841136

NSN

6505-01-284-1136

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NDC00486-1125-05

POTASSIUM PHOSPHATE,MONOBASIC,TABLETS

NSN, MFG P/N

6505012841136

NSN

6505-01-284-1136

MFG

BEACH PRODUCTS INC DBA BEACH PHARMACEUTICALS

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 852.000 MILLIGRAMS POTASSIUM PHOSPHATE, MONOBASIC ACTIVE INGREDIENT
PRIMARY CONTAINER CONTENT QUANTITY: 500.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

000768

DIFLORASONE DIACETATE CREAM,USP

NSN, MFG P/N

6505012841138

NSN

6505-01-284-1138

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000768

DIFLORASONE DIACETATE CREAM,USP

NSN, MFG P/N

6505012841138

NSN

6505-01-284-1138

MFG

ALLERGAN INC

Description

ACTIVE INGREDIENT AND STRENGTH: 0.050 DIFLORASONE DIACETATE PERCENTAGE, W/W
PRIMARY CONTAINER CONTENT QUANTITY: 60.000 GRAMS
PRIMARY CONTAINER TYPE: TUBE, COLLAPSIBLE

NDC00023-0766-60

DIFLORASONE DIACETATE CREAM,USP

NSN, MFG P/N

6505012841138

NSN

6505-01-284-1138

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NDC00023-0766-60

DIFLORASONE DIACETATE CREAM,USP

NSN, MFG P/N

6505012841138

NSN

6505-01-284-1138

MFG

ALLERGAN INC

Description

ACTIVE INGREDIENT AND STRENGTH: 0.050 DIFLORASONE DIACETATE PERCENTAGE, W/W
PRIMARY CONTAINER CONTENT QUANTITY: 60.000 GRAMS
PRIMARY CONTAINER TYPE: TUBE, COLLAPSIBLE

309530

CLOTRIMAZOLE TROCHES

NSN, MFG P/N

6505012841650

NSN

6505-01-284-1650

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309530

CLOTRIMAZOLE TROCHES

NSN, MFG P/N

6505012841650

NSN

6505-01-284-1650

MFG

BAYER PHARMACEUTICALS CORPORATION

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 10.000 MILLIGRAMS CLOTRIMAZOLE ACTIVE INGREDIENT
PRIMARY CONTAINER CONTENT QUANTITY: 14.000 TROCHES
PRIMARY CONTAINER TYPE: STRIP
TOTAL PRIMARY CONTAINER QUANTITY: 5

MYCELEX

CLOTRIMAZOLE TROCHES

NSN, MFG P/N

6505012841650

NSN

6505-01-284-1650

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MYCELEX

CLOTRIMAZOLE TROCHES

NSN, MFG P/N

6505012841650

NSN

6505-01-284-1650

MFG

BAYER PHARMACEUTICALS CORPORATION

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 10.000 MILLIGRAMS CLOTRIMAZOLE ACTIVE INGREDIENT
PRIMARY CONTAINER CONTENT QUANTITY: 14.000 TROCHES
PRIMARY CONTAINER TYPE: STRIP
TOTAL PRIMARY CONTAINER QUANTITY: 5

NDC00026-3095-38

CLOTRIMAZOLE TROCHES

NSN, MFG P/N

6505012841650

NSN

6505-01-284-1650

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NDC00026-3095-38

CLOTRIMAZOLE TROCHES

NSN, MFG P/N

6505012841650

NSN

6505-01-284-1650

MFG

BAYER PHARMACEUTICALS CORPORATION

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 10.000 MILLIGRAMS CLOTRIMAZOLE ACTIVE INGREDIENT
PRIMARY CONTAINER CONTENT QUANTITY: 14.000 TROCHES
PRIMARY CONTAINER TYPE: STRIP
TOTAL PRIMARY CONTAINER QUANTITY: 5

NDC00469-1710-60

FLUOROURACIL INJECTION,USP

NSN, MFG P/N

6505012841651

NSN

6505-01-284-1651

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NDC00469-1710-60

FLUOROURACIL INJECTION,USP

NSN, MFG P/N

6505012841651

NSN

6505-01-284-1651

MFG

LYPHOMED INC DIV OF FUJISAWA USA INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 50.000 MILLIGRAMS FLUOROURACIL ACTIVE INGREDIENT
ADMINISTRATION: INTRAVENOUS
PHARMACEUTICAL VEHICLE TYPE: AQUEOUS
PRIMARY CONTAINER CONTENT QUANTITY: 50.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL
SPECIAL FEATURES: PRESERVATIVE FREE

4HT-2DU

HEMODIALYSIS SOLUTION SET,CONCENTRATED

NSN, MFG P/N

6505012842683

NSN

6505-01-284-2683

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4HT-2DU

HEMODIALYSIS SOLUTION SET,CONCENTRATED

NSN, MFG P/N

6505012842683

NSN

6505-01-284-2683

MFG

BICARBOLYTE VIRGINIA INC

Description

COMPONENT BREAKDOWN WITHIN EACH TEST KIT: 10 1 GAL CONTAINER PART A,4;1 GAL CONTAINERS PART B,6;
SPECIAL FEATURES: EACH SET PROVIDES FOUR 4-HOUR TREATMENTS; EACH TREATMENT CONSISTS OF 2.0 GM. PER LITER OF DEXTROSE AND THE FOLLOWING MEQ. PER LITER OF IONS,SODIUM 139.0,POTASSIUM 2.0,CALCIUM 3.5,MAGNESIUM 1.5,ACETATE 4.0,BICARBONATE 35.0,AND CHLORINE 111.0

MONOCLATE

ANTIHEMOPHILIC FACTOR,USP

NSN, MFG P/N

6505012842948

NSN

6505-01-284-2948

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MONOCLATE

ANTIHEMOPHILIC FACTOR,USP

NSN, MFG P/N

6505012842948

NSN

6505-01-284-2948

MFG

ARMOUR PHARMACEUTICAL CO DIV OF RHONE-POULENC RORER INC

Description

III PART NAME ASSIGNED BY CONTROLLING AGENCY: ANTIHEMOPHILIC FACTOR USP LYOPHILIZED FORM FACTOR VIII:C HUMAN
PHYSICAL FORM: FREEZE-DRIED POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 1000.000 INTERNATIONAL UNITS OF ACTIVE INGREDIENT
PRIMARY CONTAINER TYPE: VIAL, SINGLE DOSE
SPECIAL FEATURES: FACTOR VIII:C HUMAN;HEAT TREATED,AND/OR SOLUTION/DETERGENT CONCENTRATE;EACH VIAL PACKAGED W/SUFFICIENT DILUENT,STERILE FILTER NEEDLE AND ONE WINGED INFUSION SET;1 VIAL

NDC00053-7656-04

ANTIHEMOPHILIC FACTOR,USP

NSN, MFG P/N

6505012842948

NSN

6505-01-284-2948

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NDC00053-7656-04

ANTIHEMOPHILIC FACTOR,USP

NSN, MFG P/N

6505012842948

NSN

6505-01-284-2948

MFG

CSL BEHRING L.L.C.

Description

III PART NAME ASSIGNED BY CONTROLLING AGENCY: ANTIHEMOPHILIC FACTOR USP LYOPHILIZED FORM FACTOR VIII:C HUMAN
PHYSICAL FORM: FREEZE-DRIED POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 1000.000 INTERNATIONAL UNITS OF ACTIVE INGREDIENT
PRIMARY CONTAINER TYPE: VIAL, SINGLE DOSE
SPECIAL FEATURES: FACTOR VIII:C HUMAN;HEAT TREATED,AND/OR SOLUTION/DETERGENT CONCENTRATE;EACH VIAL PACKAGED W/SUFFICIENT DILUENT,STERILE FILTER NEEDLE AND ONE WINGED INFUSION SET;1 VIAL

NDC00053-7658-04

ANTIHEMOPHILIC FACTOR,USP

NSN, MFG P/N

6505012842948

NSN

6505-01-284-2948

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NDC00053-7658-04

ANTIHEMOPHILIC FACTOR,USP

NSN, MFG P/N

6505012842948

NSN

6505-01-284-2948

MFG

ARMOUR PHARMACEUTICAL CO DIV OF RHONE-POULENC RORER INC

Description

III PART NAME ASSIGNED BY CONTROLLING AGENCY: ANTIHEMOPHILIC FACTOR USP LYOPHILIZED FORM FACTOR VIII:C HUMAN
PHYSICAL FORM: FREEZE-DRIED POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 1000.000 INTERNATIONAL UNITS OF ACTIVE INGREDIENT
PRIMARY CONTAINER TYPE: VIAL, SINGLE DOSE
SPECIAL FEATURES: FACTOR VIII:C HUMAN;HEAT TREATED,AND/OR SOLUTION/DETERGENT CONCENTRATE;EACH VIAL PACKAGED W/SUFFICIENT DILUENT,STERILE FILTER NEEDLE AND ONE WINGED INFUSION SET;1 VIAL

IMOVAX

RABIES VACCINE,USP

NSN, MFG P/N

6505012842949

NSN

6505-01-284-2949

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IMOVAX

RABIES VACCINE,USP

NSN, MFG P/N

6505012842949

NSN

6505-01-284-2949

MFG

SANOFI PASTEUR INC.

Description

III EXTERIOR CONTAINER WEIGHT: 28.50 POUNDS
III PART NAME ASSIGNED BY CONTROLLING AGENCY: RABIES VACCINE HUMAN DIPLOID CELL STRAIN SYRINGE-NEEDLE UNIT
III PROTECTIVE STORAGE FEATURE: REQUIRES REFRIGERATION BETWEEN 2 DEG TO 8 DEG C AND SUBJECT TO DAMAGE BY FREEZING
III UNIT OF ISSUE CUBE: 0.0088 CUBIC FEET
IMMEDIATE CONTAINER QUANTITY: 1
IMMEDIATE CONTAINER TYPE: SYRINGE-NEEDLE UNIT
QUANTITY WITHIN EACH IMMEDIATE CONTAINER: 1 UNIT DOSE
SPECIAL FEATURES: PACKAGE CONTAINS ONE SINGLE-DOSE DISPOSABLE SYRINGE WITH INTEGRAL NEEDLE,0.25 I.U. OF LYOPHILIZED VACCINE,AND ONE VIAL OF STERILE WATER FOR INJECTION IN SUFFICIENT QUANTITY FOR RECONSTITUTION; FOR PRE-EXPOSURE INTRADERMAL USE ONLY
UNIT PACKAGE QUANTITY: 1
UNIT PACKAGE TYPE: PACKAGE

IMOVAX RABIES ID VACCINE

RABIES VACCINE,USP

NSN, MFG P/N

6505012842949

NSN

6505-01-284-2949

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IMOVAX RABIES ID VACCINE

RABIES VACCINE,USP

NSN, MFG P/N

6505012842949

NSN

6505-01-284-2949

MFG

SANOFI PASTEUR INC.

Description

III EXTERIOR CONTAINER WEIGHT: 28.50 POUNDS
III PART NAME ASSIGNED BY CONTROLLING AGENCY: RABIES VACCINE HUMAN DIPLOID CELL STRAIN SYRINGE-NEEDLE UNIT
III PROTECTIVE STORAGE FEATURE: REQUIRES REFRIGERATION BETWEEN 2 DEG TO 8 DEG C AND SUBJECT TO DAMAGE BY FREEZING
III UNIT OF ISSUE CUBE: 0.0088 CUBIC FEET
IMMEDIATE CONTAINER QUANTITY: 1
IMMEDIATE CONTAINER TYPE: SYRINGE-NEEDLE UNIT
QUANTITY WITHIN EACH IMMEDIATE CONTAINER: 1 UNIT DOSE
SPECIAL FEATURES: PACKAGE CONTAINS ONE SINGLE-DOSE DISPOSABLE SYRINGE WITH INTEGRAL NEEDLE,0.25 I.U. OF LYOPHILIZED VACCINE,AND ONE VIAL OF STERILE WATER FOR INJECTION IN SUFFICIENT QUANTITY FOR RECONSTITUTION; FOR PRE-EXPOSURE INTRADERMAL USE ONLY
UNIT PACKAGE QUANTITY: 1
UNIT PACKAGE TYPE: PACKAGE

NDC49281-0251-20

RABIES VACCINE,USP

NSN, MFG P/N

6505012842949

NSN

6505-01-284-2949

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NDC49281-0251-20

RABIES VACCINE,USP

NSN, MFG P/N

6505012842949

NSN

6505-01-284-2949

MFG

SANOFI PASTEUR INC.

Description

III EXTERIOR CONTAINER WEIGHT: 28.50 POUNDS
III PART NAME ASSIGNED BY CONTROLLING AGENCY: RABIES VACCINE HUMAN DIPLOID CELL STRAIN SYRINGE-NEEDLE UNIT
III PROTECTIVE STORAGE FEATURE: REQUIRES REFRIGERATION BETWEEN 2 DEG TO 8 DEG C AND SUBJECT TO DAMAGE BY FREEZING
III UNIT OF ISSUE CUBE: 0.0088 CUBIC FEET
IMMEDIATE CONTAINER QUANTITY: 1
IMMEDIATE CONTAINER TYPE: SYRINGE-NEEDLE UNIT
QUANTITY WITHIN EACH IMMEDIATE CONTAINER: 1 UNIT DOSE
SPECIAL FEATURES: PACKAGE CONTAINS ONE SINGLE-DOSE DISPOSABLE SYRINGE WITH INTEGRAL NEEDLE,0.25 I.U. OF LYOPHILIZED VACCINE,AND ONE VIAL OF STERILE WATER FOR INJECTION IN SUFFICIENT QUANTITY FOR RECONSTITUTION; FOR PRE-EXPOSURE INTRADERMAL USE ONLY
UNIT PACKAGE QUANTITY: 1
UNIT PACKAGE TYPE: PACKAGE

NAPROSYN TABLETS

NAPROXEN TABLETS,USP

NSN, MFG P/N

6505012844453

NSN

6505-01-284-4453

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NAPROSYN TABLETS

NAPROXEN TABLETS,USP

NSN, MFG P/N

6505012844453

NSN

6505-01-284-4453

MFG

SYNTEX LABORATORIES INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 375.000 MILLIGRAMS NAPROXEN ACTIVE INGREDIENT
PRIMARY CONTAINER CONTENT QUANTITY: 60.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: UNIT OF USE

NDC18393-0273-02

NAPROXEN TABLETS,USP

NSN, MFG P/N

6505012844453

NSN

6505-01-284-4453

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NDC18393-0273-02

NAPROXEN TABLETS,USP

NSN, MFG P/N

6505012844453

NSN

6505-01-284-4453

MFG

SYNTEX LABORATORIES INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 375.000 MILLIGRAMS NAPROXEN ACTIVE INGREDIENT
PRIMARY CONTAINER CONTENT QUANTITY: 60.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: UNIT OF USE