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6505-01-231-7283

20 Products

RETIN-A GEL

TRETINOIN GEL,USP

NSN, MFG P/N

6505012317283

NSN

6505-01-231-7283

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RETIN-A GEL

TRETINOIN GEL,USP

NSN, MFG P/N

6505012317283

NSN

6505-01-231-7283

MFG

ORTHO DIAGNOSTIC SYSTEMS INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 0.010 PERCENTAGE, W/W RETINOIC ACID ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: TRETINOIN GEL USP 0.01% 45GM TUBE 24S
PRIMARY CONTAINER CONTENT QUANTITY: 45.000 GRAMS
PRIMARY CONTAINER TYPE: TUBE, PLASTIC SQUEEZE
TOTAL PRIMARY CONTAINER QUANTITY: 24

INDOCIN

INDOMETHACIN SUPPOSITORIES,USP

NSN, MFG P/N

6505012317284

NSN

6505-01-231-7284

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INDOCIN

INDOMETHACIN SUPPOSITORIES,USP

NSN, MFG P/N

6505012317284

NSN

6505-01-231-7284

MFG

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

Description

FEATURES PROVIDED: INDIVIDUALLY SEALED
III PART NAME ASSIGNED BY CONTROLLING AGENCY: INDOMETHACIN SUPPOSITORIES USP 50MG ADULT RECTAL I.S. 30S
PRIMARY CONTAINER TYPE: PACKAGE
SPECIAL FEATURES: 50 MG
SUPPOSITORY TYPE: ADULT RECTAL
UNIT PACKAGE QUANTITY: 30

NDC00006-0150-30

INDOMETHACIN SUPPOSITORIES,USP

NSN, MFG P/N

6505012317284

NSN

6505-01-231-7284

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NDC00006-0150-30

INDOMETHACIN SUPPOSITORIES,USP

NSN, MFG P/N

6505012317284

NSN

6505-01-231-7284

MFG

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

Description

FEATURES PROVIDED: INDIVIDUALLY SEALED
III PART NAME ASSIGNED BY CONTROLLING AGENCY: INDOMETHACIN SUPPOSITORIES USP 50MG ADULT RECTAL I.S. 30S
PRIMARY CONTAINER TYPE: PACKAGE
SPECIAL FEATURES: 50 MG
SUPPOSITORY TYPE: ADULT RECTAL
UNIT PACKAGE QUANTITY: 30

84-50

SODIUM BICARBONATE INJECTION,USP

NSN, MFG P/N

6505012317302

NSN

6505-01-231-7302

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84-50

SODIUM BICARBONATE INJECTION,USP

NSN, MFG P/N

6505012317302

NSN

6505-01-231-7302

MFG

LYPHOMED INC DIV OF FUJISAWA USA INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 7.500 PERCENTAGE, W/V SODIUM BICARBONATE ACTIVE INGREDIENT
III SUPPLEMENTARY FEATURES: MEDSEP ITEM FOR DOD,LYPHOMED INC
III THERAPEUTIC EQUIVALENT: LYPHOMED,INC
PRIMARY CONTAINER CONTENT QUANTITY: 50.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL
TOTAL PRIMARY CONTAINER QUANTITY: 25

NDC00469-8400-60

SODIUM BICARBONATE INJECTION,USP

NSN, MFG P/N

6505012317302

NSN

6505-01-231-7302

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NDC00469-8400-60

SODIUM BICARBONATE INJECTION,USP

NSN, MFG P/N

6505012317302

NSN

6505-01-231-7302

MFG

LYPHOMED INC DIV OF FUJISAWA USA INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 7.500 PERCENTAGE, W/V SODIUM BICARBONATE ACTIVE INGREDIENT
III SUPPLEMENTARY FEATURES: MEDSEP ITEM FOR DOD,LYPHOMED INC
III THERAPEUTIC EQUIVALENT: LYPHOMED,INC
PRIMARY CONTAINER CONTENT QUANTITY: 50.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL
TOTAL PRIMARY CONTAINER QUANTITY: 25

97-B1

CALCIUM GLUCONATE INJECTION,USP

NSN, MFG P/N

6505012317303

NSN

6505-01-231-7303

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97-B1

CALCIUM GLUCONATE INJECTION,USP

NSN, MFG P/N

6505012317303

NSN

6505-01-231-7303

MFG

LYPHOMED INC DIV OF FUJISAWA USA INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 94.000 MILLIGRAMS CALCIUM GLUCONATE PER MILLILITER AND MILLIGRAMS CALCIUM SACCHARATE,TETRAHYDRATE PER MILLILITER 5.000
ADMINISTRATION: INTRAMUSCULAR OR INTRAVENOUS
III THERAPEUTIC EQUIVALENT: NOT LISTED
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL
TOTAL PRIMARY CONTAINER QUANTITY: 40

NDC00469-9701-00

CALCIUM GLUCONATE INJECTION,USP

NSN, MFG P/N

6505012317303

NSN

6505-01-231-7303

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NDC00469-9701-00

CALCIUM GLUCONATE INJECTION,USP

NSN, MFG P/N

6505012317303

NSN

6505-01-231-7303

MFG

LYPHOMED INC DIV OF FUJISAWA USA INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 94.000 MILLIGRAMS CALCIUM GLUCONATE PER MILLILITER AND MILLIGRAMS CALCIUM SACCHARATE,TETRAHYDRATE PER MILLILITER 5.000
ADMINISTRATION: INTRAMUSCULAR OR INTRAVENOUS
III THERAPEUTIC EQUIVALENT: NOT LISTED
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL
TOTAL PRIMARY CONTAINER QUANTITY: 40

NDC47679-0412-52

DOCUSATE SODIUM SOLUTION,MODIFIED

NSN, MFG P/N

6505012319093

NSN

6505-01-231-9093

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NDC47679-0412-52

DOCUSATE SODIUM SOLUTION,MODIFIED

NSN, MFG P/N

6505012319093

NSN

6505-01-231-9093

MFG

BAXTER HEALTHCARE CORP PHARMACEUTICALS DIV

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: DOCUSATE SODIUM 100 MG. ACTIVE INGREDIENT
III THERAPEUTIC EQUIVALENT: NOT RATED
PRIMARY CONTAINER CONTENT QUANTITY: 10.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE, UNIT DOSE
TOTAL PRIMARY CONTAINER QUANTITY: 50

FORTAZ

CEFTAZIDIME FOR INJECTION,USP

NSN, MFG P/N

6505012319931

NSN

6505-01-231-9931

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FORTAZ

CEFTAZIDIME FOR INJECTION,USP

NSN, MFG P/N

6505012319931

NSN

6505-01-231-9931

MFG

GLAXO WELLCOME INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 500.000 GRAMS CEFTAZIDIME, ANHYDROUS EQUIVALENT
ADMINISTRATION: INTRAMUSCULAR OR INTRAVENOUS
FEATURES PROVIDED: STERILE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: CEFTAZIDIME FOR INJECTION USP 500GM VIAL 25S
III SUPPLEMENTARY FEATURES: MEDSEP ITEM FOR DOD,GLAXO INC
III THERAPEUTIC EQUIVALENT: ANY A RATED DRUG
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 500.000 GRAMS
PRIMARY CONTAINER TYPE: VIAL
TOTAL PRIMARY CONTAINER QUANTITY: 25

NDC00173-0377-31

CEFTAZIDIME FOR INJECTION,USP

NSN, MFG P/N

6505012319931

NSN

6505-01-231-9931

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NDC00173-0377-31

CEFTAZIDIME FOR INJECTION,USP

NSN, MFG P/N

6505012319931

NSN

6505-01-231-9931

MFG

GLAXO WELLCOME INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 500.000 GRAMS CEFTAZIDIME, ANHYDROUS EQUIVALENT
ADMINISTRATION: INTRAMUSCULAR OR INTRAVENOUS
FEATURES PROVIDED: STERILE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: CEFTAZIDIME FOR INJECTION USP 500GM VIAL 25S
III SUPPLEMENTARY FEATURES: MEDSEP ITEM FOR DOD,GLAXO INC
III THERAPEUTIC EQUIVALENT: ANY A RATED DRUG
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 500.000 GRAMS
PRIMARY CONTAINER TYPE: VIAL
TOTAL PRIMARY CONTAINER QUANTITY: 25

NDC17478-0102-20

TROPICAMIDE OPHTHALMIC SOLUTION,USP

NSN, MFG P/N

6505012321769

NSN

6505-01-232-1769

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NDC17478-0102-20

TROPICAMIDE OPHTHALMIC SOLUTION,USP

NSN, MFG P/N

6505012321769

NSN

6505-01-232-1769

MFG

AKORN INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 1.000 PERCENTAGE, W/V TROPICAMIDE ACTIVE INGREDIENT
ADMINISTRATION: OPHTHALMIC
FEATURES PROVIDED: STERILE
III THERAPEUTIC EQUIVALENT: NOT RATED
PHARMACEUTICAL VEHICLE TYPE: AQUEOUS
PRIMARY CONTAINER CONTENT QUANTITY: 2.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE, PLASTIC SQUEEZE
SPECIAL FEATURES: PRESERVATIVE ADDED

TROPICACYL

TROPICAMIDE OPHTHALMIC SOLUTION,USP

NSN, MFG P/N

6505012321769

NSN

6505-01-232-1769

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TROPICACYL

TROPICAMIDE OPHTHALMIC SOLUTION,USP

NSN, MFG P/N

6505012321769

NSN

6505-01-232-1769

MFG

AKORN INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 1.000 PERCENTAGE, W/V TROPICAMIDE ACTIVE INGREDIENT
ADMINISTRATION: OPHTHALMIC
FEATURES PROVIDED: STERILE
III THERAPEUTIC EQUIVALENT: NOT RATED
PHARMACEUTICAL VEHICLE TYPE: AQUEOUS
PRIMARY CONTAINER CONTENT QUANTITY: 2.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE, PLASTIC SQUEEZE
SPECIAL FEATURES: PRESERVATIVE ADDED

99-1131

METHYLPREDNISOLONE SODIUM SUCCINATE FOR INJECTION,USP

NSN, MFG P/N

6505012321987

NSN

6505-01-232-1987

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99-1131

METHYLPREDNISOLONE SODIUM SUCCINATE FOR INJECTION,USP

NSN, MFG P/N

6505012321987

NSN

6505-01-232-1987

MFG

DEFENSE LOGISTICS AGENCY DIRECTORATE OF MEDICAL MATERIEL DEFENSE SUPPLY CENTER PHILADELPHIA

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 2.000 GRAMS METHYLPREDNISOLONE EQUIVALENT
ADMINISTRATION: INTRAVENOUS
FEATURES PROVIDED: DILUENT AND STERILE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: METHYLPREDNISOLONE SOD SUCCINATE F/INJ USP 2 GRAMS IN 50ML VIAL
III THERAPEUTIC EQUIVALENT: RATED AP
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 2.000 GRAMS ACTIVE INGREDIENT
PRIMARY CONTAINER TYPE: VIAL
SPECIAL FEATURES: 2 GM. POWDER IN 50 ML. VIAL AND 30 ML. DILUENT IN SEPARATE VIAL
TOTAL PRIMARY CONTAINER QUANTITY: 2

NDC00009-0796-01

METHYLPREDNISOLONE SODIUM SUCCINATE FOR INJECTION,USP

NSN, MFG P/N

6505012321987

NSN

6505-01-232-1987

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NDC00009-0796-01

METHYLPREDNISOLONE SODIUM SUCCINATE FOR INJECTION,USP

NSN, MFG P/N

6505012321987

NSN

6505-01-232-1987

MFG

AMERISOURCEBERGEN DRUG CORPORATION DIV CORPORATE OFFICE

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 2.000 GRAMS METHYLPREDNISOLONE EQUIVALENT
ADMINISTRATION: INTRAVENOUS
FEATURES PROVIDED: DILUENT AND STERILE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: METHYLPREDNISOLONE SOD SUCCINATE F/INJ USP 2 GRAMS IN 50ML VIAL
III THERAPEUTIC EQUIVALENT: RATED AP
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 2.000 GRAMS ACTIVE INGREDIENT
PRIMARY CONTAINER TYPE: VIAL
SPECIAL FEATURES: 2 GM. POWDER IN 50 ML. VIAL AND 30 ML. DILUENT IN SEPARATE VIAL
TOTAL PRIMARY CONTAINER QUANTITY: 2

SOLU-MEDROL

METHYLPREDNISOLONE SODIUM SUCCINATE FOR INJECTION,USP

NSN, MFG P/N

6505012321987

NSN

6505-01-232-1987

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SOLU-MEDROL

METHYLPREDNISOLONE SODIUM SUCCINATE FOR INJECTION,USP

NSN, MFG P/N

6505012321987

NSN

6505-01-232-1987

MFG

PHARMACIA & UPJOHN COMPANY

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 2.000 GRAMS METHYLPREDNISOLONE EQUIVALENT
ADMINISTRATION: INTRAVENOUS
FEATURES PROVIDED: DILUENT AND STERILE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: METHYLPREDNISOLONE SOD SUCCINATE F/INJ USP 2 GRAMS IN 50ML VIAL
III THERAPEUTIC EQUIVALENT: RATED AP
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 2.000 GRAMS ACTIVE INGREDIENT
PRIMARY CONTAINER TYPE: VIAL
SPECIAL FEATURES: 2 GM. POWDER IN 50 ML. VIAL AND 30 ML. DILUENT IN SEPARATE VIAL
TOTAL PRIMARY CONTAINER QUANTITY: 2

ANGIOVIST 282

DIATRIZOATE MEGLUMINE INJECTION,USP

NSN, MFG P/N

6505012321988

NSN

6505-01-232-1988

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ANGIOVIST 282

DIATRIZOATE MEGLUMINE INJECTION,USP

NSN, MFG P/N

6505012321988

NSN

6505-01-232-1988

MFG

BAYER HEALTHCARE PHARMACEUTICALS INC. DBA BERLICHEM

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 60.000 PERCENTAGE, W/V MEGLUMINE DIATRIZOATE ACTIVE INGREDIENT
ADMINISTRATION: INTRAVENOUS
FEATURES PROVIDED: STERILE
III THERAPEUTIC EQUIVALENT: RATED AP
PHARMACEUTICAL VEHICLE TYPE: AQUEOUS
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL
TOTAL PRIMARY CONTAINER QUANTITY: 20

NDC50419-0192-10

DIATRIZOATE MEGLUMINE INJECTION,USP

NSN, MFG P/N

6505012321988

NSN

6505-01-232-1988

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NDC50419-0192-10

DIATRIZOATE MEGLUMINE INJECTION,USP

NSN, MFG P/N

6505012321988

NSN

6505-01-232-1988

MFG

BAYER HEALTHCARE PHARMACEUTICALS INC. DBA BERLICHEM

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 60.000 PERCENTAGE, W/V MEGLUMINE DIATRIZOATE ACTIVE INGREDIENT
ADMINISTRATION: INTRAVENOUS
FEATURES PROVIDED: STERILE
III THERAPEUTIC EQUIVALENT: RATED AP
PHARMACEUTICAL VEHICLE TYPE: AQUEOUS
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL
TOTAL PRIMARY CONTAINER QUANTITY: 20

NDC68516-3200-02

FACTOR IX COMPLEX,USP

NSN, MFG P/N

6505012322025

NSN

6505-01-232-2025

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NDC68516-3200-02

FACTOR IX COMPLEX,USP

NSN, MFG P/N

6505012322025

NSN

6505-01-232-2025

MFG

GRIFOLS BIOLOGICALS INC.

Description

III PART NAME ASSIGNED BY CONTROLLING AGENCY: FACTOR IX COMPLEX USP FREEZE DRIED POWDER 500 UNITS PER VIAL
III SUPPLEMENTARY FEATURES: NOTE: G,F
PHYSICAL FORM: FREEZE-DRIED POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 500.000 UNITS OF ACTIVE INGREDIENT
PRIMARY CONTAINER TYPE: VIAL
SPECIAL FEATURES: EACH PACKAGE CONTAINS:1 VIAL CONTAINING 500 UNITS (HEAT TREATED) PLUS OR MINUS 20 PCT FACTOR IX COMPLEX;STERILE FILTER NEEDLE;1 VIAL CONTAINING SUFFICIENT STERILE WATER FOR INJECTION,USP TO RECONSTITUTE THE PRODUCT

PROFILNINE

FACTOR IX COMPLEX,USP

NSN, MFG P/N

6505012322025

NSN

6505-01-232-2025

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PROFILNINE

FACTOR IX COMPLEX,USP

NSN, MFG P/N

6505012322025

NSN

6505-01-232-2025

MFG

GRIFOLS BIOLOGICALS INC.

Description

III PART NAME ASSIGNED BY CONTROLLING AGENCY: FACTOR IX COMPLEX USP FREEZE DRIED POWDER 500 UNITS PER VIAL
III SUPPLEMENTARY FEATURES: NOTE: G,F
PHYSICAL FORM: FREEZE-DRIED POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 500.000 UNITS OF ACTIVE INGREDIENT
PRIMARY CONTAINER TYPE: VIAL
SPECIAL FEATURES: EACH PACKAGE CONTAINS:1 VIAL CONTAINING 500 UNITS (HEAT TREATED) PLUS OR MINUS 20 PCT FACTOR IX COMPLEX;STERILE FILTER NEEDLE;1 VIAL CONTAINING SUFFICIENT STERILE WATER FOR INJECTION,USP TO RECONSTITUTE THE PRODUCT

ARM-A-VIAL

SODIUM CHLORIDE INHALATION SOLUTION,USP

NSN, MFG P/N

6505012323114

NSN

6505-01-232-3114

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ARM-A-VIAL

SODIUM CHLORIDE INHALATION SOLUTION,USP

NSN, MFG P/N

6505012323114

NSN

6505-01-232-3114

MFG

ARMOUR PHARMACEUTICAL CO DIV OF RORER-POULEC RORER INC

Description

PRIMARY CONTAINER CONTENT QUANTITY: 3.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL
SPECIAL FEATURES: PARABEN AND PRESERVATIVE-FREE
TOTAL PRIMARY CONTAINER QUANTITY: 100