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6505-01-104-6164

20 Products

SLO-PHYLLIN

THEOPHYLLINE TABLETS,USP

NSN, MFG P/N

6505011046164

NSN

6505-01-104-6164

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SLO-PHYLLIN

THEOPHYLLINE TABLETS,USP

NSN, MFG P/N

6505011046164

NSN

6505-01-104-6164

MFG

AVENTIS PHARMACEUTICALS PRODUCTS INC.

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 200.000 MILLIGRAMS THEOPHYLLINE ACTIVE INGREDIENT
ADMINISTRATION: ORAL
FEATURES PROVIDED: INDIVIDUALLY SEALED
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 TABLETS
PRIMARY CONTAINER TYPE: STRIP
SPECIAL FEATURES: ANHYDROUS
SUPPLEMENTARY FEATURES: MEDSEP ITEM FOR DOD,RORER PHARMACEUTICALS
THERAPEUTIC EQUIVALENT: SLO-PHYLLIN BY WM H RORER

SLO-PHILLIN TABLETS

THEOPHYLLINE TABLETS,USP

NSN, MFG P/N

6505011046164

NSN

6505-01-104-6164

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SLO-PHILLIN TABLETS

THEOPHYLLINE TABLETS,USP

NSN, MFG P/N

6505011046164

NSN

6505-01-104-6164

MFG

AVENTIS PHARMACEUTICALS PRODUCTS INC.

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 200.000 MILLIGRAMS THEOPHYLLINE ACTIVE INGREDIENT
ADMINISTRATION: ORAL
FEATURES PROVIDED: INDIVIDUALLY SEALED
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 TABLETS
PRIMARY CONTAINER TYPE: STRIP
SPECIAL FEATURES: ANHYDROUS
SUPPLEMENTARY FEATURES: MEDSEP ITEM FOR DOD,RORER PHARMACEUTICALS
THERAPEUTIC EQUIVALENT: SLO-PHYLLIN BY WM H RORER

3357

CEFOXITIN FOR INJECTION,USP

NSN, MFG P/N

6505011046393

NSN

6505-01-104-6393

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3357

CEFOXITIN FOR INJECTION,USP

NSN, MFG P/N

6505011046393

NSN

6505-01-104-6393

MFG

MERCK SHARP & DOHME CORP. DBA MERCK DIV US HUMAN HEALTH

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 2.000 GRAMS CEFOXITIN EQUIVALENT
ADMINISTRATION: INTRAMUSCULAR OR INTRAVENOUS
III PART NAME ASSIGNED BY CONTROLLING AGENCY: CEFOXITIN SODIUM STERILE USP 2GM VIAL 25S
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 2.000 GRAMS OF ACTIVE INGREDIENT
PRIMARY CONTAINER TYPE: VIAL
SPECIAL FEATURES: 20 ML. SIZE VIAL
TOTAL PRIMARY CONTAINER QUANTITY: 25

MEFOXIN

CEFOXITIN FOR INJECTION,USP

NSN, MFG P/N

6505011046393

NSN

6505-01-104-6393

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MEFOXIN

CEFOXITIN FOR INJECTION,USP

NSN, MFG P/N

6505011046393

NSN

6505-01-104-6393

MFG

MERCK SHARP & DOHME CORP. DBA MERCK DIV US HUMAN HEALTH

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 2.000 GRAMS CEFOXITIN EQUIVALENT
ADMINISTRATION: INTRAMUSCULAR OR INTRAVENOUS
III PART NAME ASSIGNED BY CONTROLLING AGENCY: CEFOXITIN SODIUM STERILE USP 2GM VIAL 25S
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 2.000 GRAMS OF ACTIVE INGREDIENT
PRIMARY CONTAINER TYPE: VIAL
SPECIAL FEATURES: 20 ML. SIZE VIAL
TOTAL PRIMARY CONTAINER QUANTITY: 25

NDC00006-3357-53

CEFOXITIN FOR INJECTION,USP

NSN, MFG P/N

6505011046393

NSN

6505-01-104-6393

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NDC00006-3357-53

CEFOXITIN FOR INJECTION,USP

NSN, MFG P/N

6505011046393

NSN

6505-01-104-6393

MFG

MERCK SHARP & DOHME CORP. DBA MERCK DIV US HUMAN HEALTH

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 2.000 GRAMS CEFOXITIN EQUIVALENT
ADMINISTRATION: INTRAMUSCULAR OR INTRAVENOUS
III PART NAME ASSIGNED BY CONTROLLING AGENCY: CEFOXITIN SODIUM STERILE USP 2GM VIAL 25S
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 2.000 GRAMS OF ACTIVE INGREDIENT
PRIMARY CONTAINER TYPE: VIAL
SPECIAL FEATURES: 20 ML. SIZE VIAL
TOTAL PRIMARY CONTAINER QUANTITY: 25

NDC59911-5964-02

CEFOXITIN FOR INJECTION,USP

NSN, MFG P/N

6505011046393

NSN

6505-01-104-6393

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NDC59911-5964-02

CEFOXITIN FOR INJECTION,USP

NSN, MFG P/N

6505011046393

NSN

6505-01-104-6393

MFG

ESI LEDERLE GENERICS

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 2.000 GRAMS CEFOXITIN EQUIVALENT
ADMINISTRATION: INTRAMUSCULAR OR INTRAVENOUS
III PART NAME ASSIGNED BY CONTROLLING AGENCY: CEFOXITIN SODIUM STERILE USP 2GM VIAL 25S
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 2.000 GRAMS OF ACTIVE INGREDIENT
PRIMARY CONTAINER TYPE: VIAL
SPECIAL FEATURES: 20 ML. SIZE VIAL
TOTAL PRIMARY CONTAINER QUANTITY: 25

NDC63323-0342-20

CEFOXITIN FOR INJECTION,USP

NSN, MFG P/N

6505011046393

NSN

6505-01-104-6393

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NDC63323-0342-20

CEFOXITIN FOR INJECTION,USP

NSN, MFG P/N

6505011046393

NSN

6505-01-104-6393

MFG

CARDINAL HEALTH INC. DBA CARDINAL HEALTH

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 2.000 GRAMS CEFOXITIN EQUIVALENT
ADMINISTRATION: INTRAMUSCULAR OR INTRAVENOUS
III PART NAME ASSIGNED BY CONTROLLING AGENCY: CEFOXITIN SODIUM STERILE USP 2GM VIAL 25S
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 2.000 GRAMS OF ACTIVE INGREDIENT
PRIMARY CONTAINER TYPE: VIAL
SPECIAL FEATURES: 20 ML. SIZE VIAL
TOTAL PRIMARY CONTAINER QUANTITY: 25

01-7430

TOLAZAMIDE TABLETS,USP

NSN, MFG P/N

6505011046408

NSN

6505-01-104-6408

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01-7430

TOLAZAMIDE TABLETS,USP

NSN, MFG P/N

6505011046408

NSN

6505-01-104-6408

MFG

GOLDLINE LABORATORIES INC. DBA GOLDLINE LABORATORIES

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 500.000 MILLIGRAMS TOLAZAMIDE ACTIVE INGREDIENT
ADMINISTRATION: ORAL
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

NDC00009-0477-06

TOLAZAMIDE TABLETS,USP

NSN, MFG P/N

6505011046408

NSN

6505-01-104-6408

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NDC00009-0477-06

TOLAZAMIDE TABLETS,USP

NSN, MFG P/N

6505011046408

NSN

6505-01-104-6408

MFG

PHARMACIA & UPJOHN COMPANY

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 500.000 MILLIGRAMS TOLAZAMIDE ACTIVE INGREDIENT
ADMINISTRATION: ORAL
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

NDC00182-1679-01

TOLAZAMIDE TABLETS,USP

NSN, MFG P/N

6505011046408

NSN

6505-01-104-6408

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NDC00182-1679-01

TOLAZAMIDE TABLETS,USP

NSN, MFG P/N

6505011046408

NSN

6505-01-104-6408

MFG

GOLDLINE LABORATORIES INC. DBA GOLDLINE LABORATORIES

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 500.000 MILLIGRAMS TOLAZAMIDE ACTIVE INGREDIENT
ADMINISTRATION: ORAL
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

TOLINASE

TOLAZAMIDE TABLETS,USP

NSN, MFG P/N

6505011046408

NSN

6505-01-104-6408

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TOLINASE

TOLAZAMIDE TABLETS,USP

NSN, MFG P/N

6505011046408

NSN

6505-01-104-6408

MFG

PHARMACIA & UPJOHN COMPANY

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 500.000 MILLIGRAMS TOLAZAMIDE ACTIVE INGREDIENT
ADMINISTRATION: ORAL
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

E.E.S.

ERYTHROMYCIN ETHYLSUCCINATE FOR ORAL SUSPENSION,USP

NSN, MFG P/N

6505011047716

NSN

6505-01-104-7716

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E.E.S.

ERYTHROMYCIN ETHYLSUCCINATE FOR ORAL SUSPENSION,USP

NSN, MFG P/N

6505011047716

NSN

6505-01-104-7716

MFG

ABBOTT LABORATORIES PHARMACEUTICAL PRODUCTS DIV

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 200.000 MILLIGRAMS ERYTHROMYCIN EQUIVALENT PER 5 MILLILITERS OF RECONSTITUTED SUSPENSION
FLAVOR: CHERRY
III SUPPLEMENTARY FEATURES: MEDSEP ITEM FOR DOD,ABBOTT LABS
PHYSICAL FORM: GRANULE
PRIMARY CONTAINER CONTENT QUANTITY: 60.000 MILLILITERS AFTER RECONSTITUTION
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: DO NOT REFRIGERATE

E.E.S. GRANULES

ERYTHROMYCIN ETHYLSUCCINATE FOR ORAL SUSPENSION,USP

NSN, MFG P/N

6505011047716

NSN

6505-01-104-7716

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E.E.S. GRANULES

ERYTHROMYCIN ETHYLSUCCINATE FOR ORAL SUSPENSION,USP

NSN, MFG P/N

6505011047716

NSN

6505-01-104-7716

MFG

ABBOTT LABORATORIES PHARMACEUTICAL PRODUCTS DIV

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 200.000 MILLIGRAMS ERYTHROMYCIN EQUIVALENT PER 5 MILLILITERS OF RECONSTITUTED SUSPENSION
FLAVOR: CHERRY
III SUPPLEMENTARY FEATURES: MEDSEP ITEM FOR DOD,ABBOTT LABS
PHYSICAL FORM: GRANULE
PRIMARY CONTAINER CONTENT QUANTITY: 60.000 MILLILITERS AFTER RECONSTITUTION
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: DO NOT REFRIGERATE

NDC00074-6369-01

ERYTHROMYCIN ETHYLSUCCINATE FOR ORAL SUSPENSION,USP

NSN, MFG P/N

6505011047716

NSN

6505-01-104-7716

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NDC00074-6369-01

ERYTHROMYCIN ETHYLSUCCINATE FOR ORAL SUSPENSION,USP

NSN, MFG P/N

6505011047716

NSN

6505-01-104-7716

MFG

ABBOTT LABORATORIES PHARMACEUTICAL PRODUCTS DIV

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 200.000 MILLIGRAMS ERYTHROMYCIN EQUIVALENT PER 5 MILLILITERS OF RECONSTITUTED SUSPENSION
FLAVOR: CHERRY
III SUPPLEMENTARY FEATURES: MEDSEP ITEM FOR DOD,ABBOTT LABS
PHYSICAL FORM: GRANULE
PRIMARY CONTAINER CONTENT QUANTITY: 60.000 MILLILITERS AFTER RECONSTITUTION
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: DO NOT REFRIGERATE

2608-02

HYDROCHLORIC ACID,DILUTED,NF

NSN, MFG P/N

6505011050426

NSN

6505-01-105-0426

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2608-02

HYDROCHLORIC ACID,DILUTED,NF

NSN, MFG P/N

6505011050426

NSN

6505-01-105-0426

MFG

MALLINCKRODT INC ANESTHESIA PRODUCTS

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 10.000 PERCENTAGE, W/V HYDROCHLORIC ACID ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: HYDROCHLORIC ACID DILUTED NF 473ML BT
III PROTECTIVE STORAGE FEATURE: CORROSIVE
PHARMACEUTICAL VEHICLE TYPE: AQUEOUS
PRIMARY CONTAINER CONTENT QUANTITY: 473.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE

000261

DIPIVEFRIN HYDROCHLORIDE OPHTHALMIC SOLUTION,USP

NSN, MFG P/N

6505011051264

NSN

6505-01-105-1264

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000261

DIPIVEFRIN HYDROCHLORIDE OPHTHALMIC SOLUTION,USP

NSN, MFG P/N

6505011051264

NSN

6505-01-105-1264

MFG

ALLERGAN INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 0.100 PERCENTAGE, W/V DIPIVEFRIN HYDROCHLORIDE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: DIPIVEFRIN HYDROCHLORIDE OPHTHALMIC SOLUTION 0.1% 10ML BT
PHARMACEUTICAL VEHICLE TYPE: AQUEOUS
PRIMARY CONTAINER CONTENT QUANTITY: 10.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE WITH DROPPER, PLASTIC SQUEEZE
SPECIAL FEATURES: WITH PRESERVATIVES AND WETTING AGENTS

4924

DIPIVEFRIN HYDROCHLORIDE OPHTHALMIC SOLUTION,USP

NSN, MFG P/N

6505011051264

NSN

6505-01-105-1264

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4924

DIPIVEFRIN HYDROCHLORIDE OPHTHALMIC SOLUTION,USP

NSN, MFG P/N

6505011051264

NSN

6505-01-105-1264

MFG

ALLERGAN INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 0.100 PERCENTAGE, W/V DIPIVEFRIN HYDROCHLORIDE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: DIPIVEFRIN HYDROCHLORIDE OPHTHALMIC SOLUTION 0.1% 10ML BT
PHARMACEUTICAL VEHICLE TYPE: AQUEOUS
PRIMARY CONTAINER CONTENT QUANTITY: 10.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE WITH DROPPER, PLASTIC SQUEEZE
SPECIAL FEATURES: WITH PRESERVATIVES AND WETTING AGENTS

NDC00023-9208-10

DIPIVEFRIN HYDROCHLORIDE OPHTHALMIC SOLUTION,USP

NSN, MFG P/N

6505011051264

NSN

6505-01-105-1264

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NDC00023-9208-10

DIPIVEFRIN HYDROCHLORIDE OPHTHALMIC SOLUTION,USP

NSN, MFG P/N

6505011051264

NSN

6505-01-105-1264

MFG

ALLERGAN INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 0.100 PERCENTAGE, W/V DIPIVEFRIN HYDROCHLORIDE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: DIPIVEFRIN HYDROCHLORIDE OPHTHALMIC SOLUTION 0.1% 10ML BT
PHARMACEUTICAL VEHICLE TYPE: AQUEOUS
PRIMARY CONTAINER CONTENT QUANTITY: 10.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE WITH DROPPER, PLASTIC SQUEEZE
SPECIAL FEATURES: WITH PRESERVATIVES AND WETTING AGENTS

NDC00364-3040-54

DIPIVEFRIN HYDROCHLORIDE OPHTHALMIC SOLUTION,USP

NSN, MFG P/N

6505011051264

NSN

6505-01-105-1264

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NDC00364-3040-54

DIPIVEFRIN HYDROCHLORIDE OPHTHALMIC SOLUTION,USP

NSN, MFG P/N

6505011051264

NSN

6505-01-105-1264

MFG

SCHEIN PHARMACEUTICAL INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 0.100 PERCENTAGE, W/V DIPIVEFRIN HYDROCHLORIDE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: DIPIVEFRIN HYDROCHLORIDE OPHTHALMIC SOLUTION 0.1% 10ML BT
PHARMACEUTICAL VEHICLE TYPE: AQUEOUS
PRIMARY CONTAINER CONTENT QUANTITY: 10.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE WITH DROPPER, PLASTIC SQUEEZE
SPECIAL FEATURES: WITH PRESERVATIVES AND WETTING AGENTS

NDC11980-0260-20

DIPIVEFRIN HYDROCHLORIDE OPHTHALMIC SOLUTION,USP

NSN, MFG P/N

6505011051264

NSN

6505-01-105-1264

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NDC11980-0260-20

DIPIVEFRIN HYDROCHLORIDE OPHTHALMIC SOLUTION,USP

NSN, MFG P/N

6505011051264

NSN

6505-01-105-1264

MFG

ALLERGAN INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 0.100 PERCENTAGE, W/V DIPIVEFRIN HYDROCHLORIDE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: DIPIVEFRIN HYDROCHLORIDE OPHTHALMIC SOLUTION 0.1% 10ML BT
PHARMACEUTICAL VEHICLE TYPE: AQUEOUS
PRIMARY CONTAINER CONTENT QUANTITY: 10.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE WITH DROPPER, PLASTIC SQUEEZE
SPECIAL FEATURES: WITH PRESERVATIVES AND WETTING AGENTS