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6505-01-174-4069

20 Products

NDC00053-1219-33

MULTIVITAMIN SOLUTION FOR INJECTION

NSN, MFG P/N

6505011744069

NSN

6505-01-174-4069

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NDC00053-1219-33

MULTIVITAMIN SOLUTION FOR INJECTION

NSN, MFG P/N

6505011744069

NSN

6505-01-174-4069

MFG

ARMOUR PHARMACEUTICAL CO DIV OF RORER-POULEC RORER INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 500.000 MILLIGRAMS ASCORBIC ACID ACTIVE INGREDIENT AND 25.000 MILLIGRAMS DEXPANTHENOL ACTIVE INGREDIENT AND 25.000 MICROGRAMS ERGOCALCIFEROL ACTIVE INGREDIENT AND 100.000 MILLIGRAMS NIACINAMIDE ACTIVE INGREDIENT AND 15.000 MILLIGRAMS PYRIDOXINE
PRIMARY CONTAINER CONTENT QUANTITY: 5.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL
SPECIAL FEATURES: TO BE DILUTED WITH NOT LESS THAN 500 ML INFUSION FLUID
~1: HYDROCHLORIDE ACTIVE INGREDIENT AND 10.000 MILLIGRAMS RIBOFLAVIN ACTIVE INGREDIENT AND 50.000 MILLIGRAMS THIAMINE ACTIVE INGREDIENT AND 3.000 MILLIGRAMS VITAMIN A ACTIVE INGREDIENT AND 5.000 MILLIGRAMS VITAMIN E ACTIVE INGREDIENT

01-7013

SULFASALAZINE TABLETS,USP

NSN, MFG P/N

6505011744988

NSN

6505-01-174-4988

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01-7013

SULFASALAZINE TABLETS,USP

NSN, MFG P/N

6505011744988

NSN

6505-01-174-4988

MFG

GOLDLINE LABORATORIES INC. DBA GOLDLINE LABORATORIES

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 500.000 MILLIGRAMS SULFASALAZINE ACTIVE INGREDIENT
PRIMARY CONTAINER CONTENT QUANTITY: 1000.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

NDC00032-2060-10

SULFASALAZINE TABLETS,USP

NSN, MFG P/N

6505011744988

NSN

6505-01-174-4988

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NDC00032-2060-10

SULFASALAZINE TABLETS,USP

NSN, MFG P/N

6505011744988

NSN

6505-01-174-4988

MFG

SOLVAY PHARMACEUTICALS INC.

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 500.000 MILLIGRAMS SULFASALAZINE ACTIVE INGREDIENT
PRIMARY CONTAINER CONTENT QUANTITY: 1000.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

NDC00182-1016-10

SULFASALAZINE TABLETS,USP

NSN, MFG P/N

6505011744988

NSN

6505-01-174-4988

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NDC00182-1016-10

SULFASALAZINE TABLETS,USP

NSN, MFG P/N

6505011744988

NSN

6505-01-174-4988

MFG

GOLDLINE LABORATORIES INC. DBA GOLDLINE LABORATORIES

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 500.000 MILLIGRAMS SULFASALAZINE ACTIVE INGREDIENT
PRIMARY CONTAINER CONTENT QUANTITY: 1000.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

NDC00223-1727-02

SULFASALAZINE TABLETS,USP

NSN, MFG P/N

6505011744988

NSN

6505-01-174-4988

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NDC00223-1727-02

SULFASALAZINE TABLETS,USP

NSN, MFG P/N

6505011744988

NSN

6505-01-174-4988

MFG

CONSOLIDATED MIDLAND CORP

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 500.000 MILLIGRAMS SULFASALAZINE ACTIVE INGREDIENT
PRIMARY CONTAINER CONTENT QUANTITY: 1000.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

ALBUMINAR-5

ALBUMIN HUMAN,USP

NSN, MFG P/N

6505011744990

NSN

6505-01-174-4990

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ALBUMINAR-5

ALBUMIN HUMAN,USP

NSN, MFG P/N

6505011744990

NSN

6505-01-174-4990

MFG

ARMOUR PHARMACEUTICAL CO DIV OF RORER-POULEC RORER INC

Description

PRIMARY CONTAINER CONTENT QUANTITY: 1000.000 MILLILITERS
SPECIAL FEATURES: FOR USE WITH AN INTRAVENOUS ADMINISTRATION SET (INCLUDED);5.0000 PERCENT PER 100 MILLILITERS
TOTAL PRIMARY CONTAINER QUANTITY: 1

NDC00053-7670-03

ALBUMIN HUMAN,USP

NSN, MFG P/N

6505011744990

NSN

6505-01-174-4990

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NDC00053-7670-03

ALBUMIN HUMAN,USP

NSN, MFG P/N

6505011744990

NSN

6505-01-174-4990

MFG

ARMOUR PHARMACEUTICAL CO DIV OF RORER-POULEC RORER INC

Description

PRIMARY CONTAINER CONTENT QUANTITY: 1000.000 MILLILITERS
SPECIAL FEATURES: FOR USE WITH AN INTRAVENOUS ADMINISTRATION SET (INCLUDED);5.0000 PERCENT PER 100 MILLILITERS
TOTAL PRIMARY CONTAINER QUANTITY: 1

BSS PLUS

OPHTHALMIC IRRIGATING SOLUTION

NSN, MFG P/N

6505011745842

NSN

6505-01-174-5842

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BSS PLUS

OPHTHALMIC IRRIGATING SOLUTION

NSN, MFG P/N

6505011745842

NSN

6505-01-174-5842

MFG

ALCON LABORATORIES INC .

Description

ADMINISTRATION: OPHTHALMIC IRRIGATION
FEATURES PROVIDED: STERILE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: OPHTHALMIC IRRIGATING SOLUTION 500ML BOTTLE 6S
III THERAPEUTIC EQUIVALENT: BSS PLUS BY ALCON
PRIMARY CONTAINER CONTENT QUANTITY: 500.000 MILLILITERS OR 515.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: FOR INTRAOCULAR USE; SHALL CONSIST OF TWO PARTS (PART I AND PART II), SUCH THAT WHEN MIXED TOGETHER, EACH ML OF THE RECONSTITUTED PRODUCT CONTAINS 7.14 MG SODIUM CHLORIDE, 0.38 MG POTASSIUM CHLORIDE, 0.154 MG CALCIUM CHLORIDE DIHYDRATE, 0.42 MGDIBASIC
TOTAL PRIMARY CONTAINER QUANTITY: 6
~1: SODIUM PHOSPHATE (ANHYDROUS), 0.20 MG MAGNESIUM CHLORIDE HEXAHYDRATE, 2.1 MG SODIUM BICARBONATE, 0.92 MG DEXTROSE, 0.184 MG GLUTATHIONE DISULFIDE (OXIDIZED GLUTATHIONE), HYDROCHLORIC ACID AND/OR SODIUM HYDROXIDE (TO ADJUST PH), IN WATER FOR INJECTION; THE
~2: RECONSTITUTED PRODUCT HAS APPROXIMATE PH OF 7.4 AND OSMOLARITY OF APPOXIMATELEY 305 MOSMOL PER LITER; THE UNIT OF ISSUE SHALL BE EITHER SIX 500 ML BTS CONTAINING PART I WITH SIX 20 ML BTS CONTAINING PART II CONCENTRATE OR SIX 515 ML BTS CONTAINING PART I
~3: WITH SIX VIALS CONTAINING LYOPILIZED POWDER FOR PART II, TOGETHER WITH SIX STERILE TRANSFER SPIKES

NDC00023-0005-51

OPHTHALMIC IRRIGATING SOLUTION

NSN, MFG P/N

6505011745842

NSN

6505-01-174-5842

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NDC00023-0005-51

OPHTHALMIC IRRIGATING SOLUTION

NSN, MFG P/N

6505011745842

NSN

6505-01-174-5842

MFG

ALLERGAN INC

Description

ADMINISTRATION: OPHTHALMIC IRRIGATION
FEATURES PROVIDED: STERILE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: OPHTHALMIC IRRIGATING SOLUTION 500ML BOTTLE 6S
III THERAPEUTIC EQUIVALENT: BSS PLUS BY ALCON
PRIMARY CONTAINER CONTENT QUANTITY: 500.000 MILLILITERS OR 515.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: FOR INTRAOCULAR USE; SHALL CONSIST OF TWO PARTS (PART I AND PART II), SUCH THAT WHEN MIXED TOGETHER, EACH ML OF THE RECONSTITUTED PRODUCT CONTAINS 7.14 MG SODIUM CHLORIDE, 0.38 MG POTASSIUM CHLORIDE, 0.154 MG CALCIUM CHLORIDE DIHYDRATE, 0.42 MGDIBASIC
TOTAL PRIMARY CONTAINER QUANTITY: 6
~1: SODIUM PHOSPHATE (ANHYDROUS), 0.20 MG MAGNESIUM CHLORIDE HEXAHYDRATE, 2.1 MG SODIUM BICARBONATE, 0.92 MG DEXTROSE, 0.184 MG GLUTATHIONE DISULFIDE (OXIDIZED GLUTATHIONE), HYDROCHLORIC ACID AND/OR SODIUM HYDROXIDE (TO ADJUST PH), IN WATER FOR INJECTION; THE
~2: RECONSTITUTED PRODUCT HAS APPROXIMATE PH OF 7.4 AND OSMOLARITY OF APPOXIMATELEY 305 MOSMOL PER LITER; THE UNIT OF ISSUE SHALL BE EITHER SIX 500 ML BTS CONTAINING PART I WITH SIX 20 ML BTS CONTAINING PART II CONCENTRATE OR SIX 515 ML BTS CONTAINING PART I
~3: WITH SIX VIALS CONTAINING LYOPILIZED POWDER FOR PART II, TOGETHER WITH SIX STERILE TRANSFER SPIKES

NDC00065-0800-50

OPHTHALMIC IRRIGATING SOLUTION

NSN, MFG P/N

6505011745842

NSN

6505-01-174-5842

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NDC00065-0800-50

OPHTHALMIC IRRIGATING SOLUTION

NSN, MFG P/N

6505011745842

NSN

6505-01-174-5842

MFG

ALCON LABORATORIES INC .

Description

ADMINISTRATION: OPHTHALMIC IRRIGATION
FEATURES PROVIDED: STERILE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: OPHTHALMIC IRRIGATING SOLUTION 500ML BOTTLE 6S
III THERAPEUTIC EQUIVALENT: BSS PLUS BY ALCON
PRIMARY CONTAINER CONTENT QUANTITY: 500.000 MILLILITERS OR 515.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: FOR INTRAOCULAR USE; SHALL CONSIST OF TWO PARTS (PART I AND PART II), SUCH THAT WHEN MIXED TOGETHER, EACH ML OF THE RECONSTITUTED PRODUCT CONTAINS 7.14 MG SODIUM CHLORIDE, 0.38 MG POTASSIUM CHLORIDE, 0.154 MG CALCIUM CHLORIDE DIHYDRATE, 0.42 MGDIBASIC
TOTAL PRIMARY CONTAINER QUANTITY: 6
~1: SODIUM PHOSPHATE (ANHYDROUS), 0.20 MG MAGNESIUM CHLORIDE HEXAHYDRATE, 2.1 MG SODIUM BICARBONATE, 0.92 MG DEXTROSE, 0.184 MG GLUTATHIONE DISULFIDE (OXIDIZED GLUTATHIONE), HYDROCHLORIC ACID AND/OR SODIUM HYDROXIDE (TO ADJUST PH), IN WATER FOR INJECTION; THE
~2: RECONSTITUTED PRODUCT HAS APPROXIMATE PH OF 7.4 AND OSMOLARITY OF APPOXIMATELEY 305 MOSMOL PER LITER; THE UNIT OF ISSUE SHALL BE EITHER SIX 500 ML BTS CONTAINING PART I WITH SIX 20 ML BTS CONTAINING PART II CONCENTRATE OR SIX 515 ML BTS CONTAINING PART I
~3: WITH SIX VIALS CONTAINING LYOPILIZED POWDER FOR PART II, TOGETHER WITH SIX STERILE TRANSFER SPIKES

NDC00039-0019-11

CEFOTAXIME SODIUM,USP

NSN, MFG P/N

6505011749915

NSN

6505-01-174-9915

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NDC00039-0019-11

CEFOTAXIME SODIUM,USP

NSN, MFG P/N

6505011749915

NSN

6505-01-174-9915

MFG

HOECHST-ROUSSEL PHARMACEUTICALS INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 2.000 GRAMS CEFOTAXIME EQUIVALENT
ADMINISTRATION: INTRAVENOUS
III PART NAME ASSIGNED BY CONTROLLING AGENCY: CEFOTAXIME SODIUM STERILE USP 2GM BOTTLE 10S
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 2.000 GRAMS
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: IN AN OVERSIZED BT W/A RATED CAPACITY OF NOT LESS THAN 100ML
TOTAL PRIMARY CONTAINER QUANTITY: 10

FP-R-3 SINGLE KIT

ANTIDOTE TREATMENT KIT,NERVE AGENT

NSN, MFG P/N

6505011749919

NSN

6505-01-174-9919

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FP-R-3 SINGLE KIT

ANTIDOTE TREATMENT KIT,NERVE AGENT

NSN, MFG P/N

6505011749919

NSN

6505-01-174-9919

MFG

MERIDIAN MEDICAL TECHNOLOGIES INC.

Description

III PART NAME ASSIGNED BY CONTROLLING AGENCY: ANTIDOTE TREATMENT KIT NERVE AGENT
SPECIAL FEATURES: EITHER INJECTOR SHALL BE ARMED AND READY FOR ADMINISTRATION WHEN REMOVED FROM THE HOLDER; KIT COMPONENTS SHALL BE REPLACEABLE
TEST CAPABILITY QUANTITY: 1
USAGE DESIGN: FOR USE AS AN ANTIDOTE FOR NERVE GAS

MARK I

ANTIDOTE TREATMENT KIT,NERVE AGENT

NSN, MFG P/N

6505011749919

NSN

6505-01-174-9919

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MARK I

ANTIDOTE TREATMENT KIT,NERVE AGENT

NSN, MFG P/N

6505011749919

NSN

6505-01-174-9919

MFG

MERIDIAN MEDICAL TECHNOLOGIES INC.

Description

III PART NAME ASSIGNED BY CONTROLLING AGENCY: ANTIDOTE TREATMENT KIT NERVE AGENT
SPECIAL FEATURES: EITHER INJECTOR SHALL BE ARMED AND READY FOR ADMINISTRATION WHEN REMOVED FROM THE HOLDER; KIT COMPONENTS SHALL BE REPLACEABLE
TEST CAPABILITY QUANTITY: 1
USAGE DESIGN: FOR USE AS AN ANTIDOTE FOR NERVE GAS

P0125

POLYETHYLENE GLYCOL,NF

NSN, MFG P/N

6505011749926

NSN

6505-01-174-9926

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P0125

POLYETHYLENE GLYCOL,NF

NSN, MFG P/N

6505011749926

NSN

6505-01-174-9926

MFG

SPECTRUM LABORATORY PRODUCTS INC. DBA SPECTRUM CHEMICALS AND LABORATORY PRODUCTS

Description

III PART NAME ASSIGNED BY CONTROLLING AGENCY: POLYETHYLENE GLYCOL NF POWDER FORM 1LB JAR
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 1.000 POUNDS
PRIMARY CONTAINER TYPE: JAR, GLASS

NDC00068-0104-61

PSEUDOEPHEDRINE HYDROCHLORIDE EXTENDED-RELEASE CAPSULES

NSN, MFG P/N

6505011749930

NSN

6505-01-174-9930

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NDC00068-0104-61

PSEUDOEPHEDRINE HYDROCHLORIDE EXTENDED-RELEASE CAPSULES

NSN, MFG P/N

6505011749930

NSN

6505-01-174-9930

MFG

MERRELL DOW PHARMECEUTICALS INC BIDS AND CONTRACTS DEPT

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 120.000 MILLIGRAMS PSEUDOEPHEDRINE HYDROCHLORIDE ACTIVE INGREDIENT
CAPSULE CONTENT FORM: ANY ACCEPTABLE
CAPSULE PRIMARY CONTAINER CONTENT QUANTITY: 100.000
CAPSULE TYPE: ANY ACCEPTABLE
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: SHALL PROVIDE CONTINUOUS THERAPEUTIC EFFECT FOR 12 HOURS

NOVAFED

PSEUDOEPHEDRINE HYDROCHLORIDE EXTENDED-RELEASE CAPSULES

NSN, MFG P/N

6505011749930

NSN

6505-01-174-9930

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NOVAFED

PSEUDOEPHEDRINE HYDROCHLORIDE EXTENDED-RELEASE CAPSULES

NSN, MFG P/N

6505011749930

NSN

6505-01-174-9930

MFG

MERRELL DOW PHARMECEUTICALS INC BIDS AND CONTRACTS DEPT

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 120.000 MILLIGRAMS PSEUDOEPHEDRINE HYDROCHLORIDE ACTIVE INGREDIENT
CAPSULE CONTENT FORM: ANY ACCEPTABLE
CAPSULE PRIMARY CONTAINER CONTENT QUANTITY: 100.000
CAPSULE TYPE: ANY ACCEPTABLE
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: SHALL PROVIDE CONTINUOUS THERAPEUTIC EFFECT FOR 12 HOURS

NDC00168-0020-31

HYDROCORTISONE OINTMENT,USP

NSN, MFG P/N

6505011749931

NSN

6505-01-174-9931

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NDC00168-0020-31

HYDROCORTISONE OINTMENT,USP

NSN, MFG P/N

6505011749931

NSN

6505-01-174-9931

MFG

CARDINAL HEALTH INC. DBA CARDINAL HEALTH

Description

ACTIVE INGREDIENT AND STRENGTH: 1.000 HYDROCORTISONE PERCENTAGE, W/W
ADMINISTRATION: TOPICAL
III PART NAME ASSIGNED BY CONTROLLING AGENCY: HYDROCORTISONE OINTMENT 1% TOPICAL 1OZ TUBE
PRIMARY CONTAINER CONTENT QUANTITY: 1.000 OUNCES
PRIMARY CONTAINER TYPE: TUBE, COLLAPSIBLE

NDC00143-9979-22

CEFUROXIME SODIUM,USP

NSN, MFG P/N

6505011751228

NSN

6505-01-175-1228

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NDC00143-9979-22

CEFUROXIME SODIUM,USP

NSN, MFG P/N

6505011751228

NSN

6505-01-175-1228

MFG

WEST-WARD PHARMACEUTICAL CORP

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 750.000 MILLIGRAMS CEFUROXIME EQUIVALENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: CEFUROXIME SODIUM STERILE 750MG VIAL 25S
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 750.000 MILLIGRAMS OF ACTIVE INGREDIENT
PRIMARY CONTAINER TYPE: VIAL
TOTAL PRIMARY CONTAINER QUANTITY: 25

NDC10019-0620-01

CEFUROXIME SODIUM,USP

NSN, MFG P/N

6505011751228

NSN

6505-01-175-1228

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NDC10019-0620-01

CEFUROXIME SODIUM,USP

NSN, MFG P/N

6505011751228

NSN

6505-01-175-1228

MFG

BAXTER HEALTHCARE CORP SCIENTIFIC TECHNICAL SYSTEMS DIV

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 750.000 MILLIGRAMS CEFUROXIME EQUIVALENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: CEFUROXIME SODIUM STERILE 750MG VIAL 25S
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 750.000 MILLIGRAMS OF ACTIVE INGREDIENT
PRIMARY CONTAINER TYPE: VIAL
TOTAL PRIMARY CONTAINER QUANTITY: 25

ZINACEF

CEFUROXIME SODIUM,USP

NSN, MFG P/N

6505011751228

NSN

6505-01-175-1228

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ZINACEF

CEFUROXIME SODIUM,USP

NSN, MFG P/N

6505011751228

NSN

6505-01-175-1228

MFG

GLAXO WELLCOME INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 750.000 MILLIGRAMS CEFUROXIME EQUIVALENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: CEFUROXIME SODIUM STERILE 750MG VIAL 25S
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 750.000 MILLIGRAMS OF ACTIVE INGREDIENT
PRIMARY CONTAINER TYPE: VIAL
TOTAL PRIMARY CONTAINER QUANTITY: 25