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6505-01-215-4147

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NDC11940-0103-06

OINTMENT BASE

NSN, MFG P/N

6505012154147

NSN

6505-01-215-4147

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NDC11940-0103-06

OINTMENT BASE

NSN, MFG P/N

6505012154147

NSN

6505-01-215-4147

MFG

MEDCO LAB INC

Description

PRIMARY CONTAINER CONTENT QUANTITY: 1.000 POUNDS
PRIMARY CONTAINER TYPE: JAR
SPECIAL FEATURES: CONTAINS STEARYL ALCOHOL,WHITE PETROLATUM,ISOPROPYL PALMITATE,SORBITOL,PROPYLENE GLYCOL,SODIUM LAURYL SULFATE,METHYLPARABEN,AND PROPYLPARABEN

NDC16837-0610-12

ALUMINA,MAGNESIA,AND SIMETHICONE ORAL SUSPENSION,USP

NSN, MFG P/N

6505012154148

NSN

6505-01-215-4148

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NDC16837-0610-12

ALUMINA,MAGNESIA,AND SIMETHICONE ORAL SUSPENSION,USP

NSN, MFG P/N

6505012154148

NSN

6505-01-215-4148

MFG

DPL ACE

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 40.000 MILLIGRAMS ALUMINUM HYDROXIDE GEL PER MILLILITER AND 40.000 MILLIGRAMS MAGNESIUM HYDROXIDE PER MILLILITER AND 4.000 TO 5.000 MG SIMETHICONE PER ML
III PART NAME ASSIGNED BY CONTROLLING AGENCY: ALUMINUM MAGNESIUM HYDROXIDE GEL & SIMETHICONE SUSPENSION 12 FL OZ
PRIMARY CONTAINER CONTENT QUANTITY: 12.000 FLUID OUNCES
PRIMARY CONTAINER TYPE: BOTTLE

NDC00469-3300-60

POTASSIUM ACETATE INJECTION,USP

NSN, MFG P/N

6505012154150

NSN

6505-01-215-4150

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NDC00469-3300-60

POTASSIUM ACETATE INJECTION,USP

NSN, MFG P/N

6505012154150

NSN

6505-01-215-4150

MFG

LYPHOMED INC DIV OF FUJISAWA USA INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 4.000 MILLIEQUIVALENTS POTASSIUM ACETATE PER MILLILITER
III PART NAME ASSIGNED BY CONTROLLING AGENCY: POTASSIUM ACETATE INJECTION USP 4MEG/ML 50ML VIAL 25S PG
PRIMARY CONTAINER CONTENT QUANTITY: 50.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL, SINGLE DOSE
TOTAL PRIMARY CONTAINER QUANTITY: 25

NDC00517-5024-25

POTASSIUM ACETATE INJECTION,USP

NSN, MFG P/N

6505012154150

NSN

6505-01-215-4150

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NDC00517-5024-25

POTASSIUM ACETATE INJECTION,USP

NSN, MFG P/N

6505012154150

NSN

6505-01-215-4150

MFG

LUITPOLD PHARMACEUTICALS INC OSTEOHEALTH COMPANY OSTEOHEALTH DIV

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 4.000 MILLIEQUIVALENTS POTASSIUM ACETATE PER MILLILITER
III PART NAME ASSIGNED BY CONTROLLING AGENCY: POTASSIUM ACETATE INJECTION USP 4MEG/ML 50ML VIAL 25S PG
PRIMARY CONTAINER CONTENT QUANTITY: 50.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL, SINGLE DOSE
TOTAL PRIMARY CONTAINER QUANTITY: 25

NDC00686-5024-25

POTASSIUM ACETATE INJECTION,USP

NSN, MFG P/N

6505012154150

NSN

6505-01-215-4150

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NDC00686-5024-25

POTASSIUM ACETATE INJECTION,USP

NSN, MFG P/N

6505012154150

NSN

6505-01-215-4150

MFG

RAWAY PHARMACAL INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 4.000 MILLIEQUIVALENTS POTASSIUM ACETATE PER MILLILITER
III PART NAME ASSIGNED BY CONTROLLING AGENCY: POTASSIUM ACETATE INJECTION USP 4MEG/ML 50ML VIAL 25S PG
PRIMARY CONTAINER CONTENT QUANTITY: 50.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL, SINGLE DOSE
TOTAL PRIMARY CONTAINER QUANTITY: 25

NDC63323-0033-50

POTASSIUM ACETATE INJECTION,USP

NSN, MFG P/N

6505012154150

NSN

6505-01-215-4150

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NDC63323-0033-50

POTASSIUM ACETATE INJECTION,USP

NSN, MFG P/N

6505012154150

NSN

6505-01-215-4150

MFG

AMERICAN PHARMACEUTICAL PARTNERS

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 4.000 MILLIEQUIVALENTS POTASSIUM ACETATE PER MILLILITER
III PART NAME ASSIGNED BY CONTROLLING AGENCY: POTASSIUM ACETATE INJECTION USP 4MEG/ML 50ML VIAL 25S PG
PRIMARY CONTAINER CONTENT QUANTITY: 50.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL, SINGLE DOSE
TOTAL PRIMARY CONTAINER QUANTITY: 25

NDC00028-0042-01

THEOPHYLLINE EXTENDED-RELEASE TABLETS

NSN, MFG P/N

6505012154389

NSN

6505-01-215-4389

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NDC00028-0042-01

THEOPHYLLINE EXTENDED-RELEASE TABLETS

NSN, MFG P/N

6505012154389

NSN

6505-01-215-4389

MFG

CIBA-GEIGY CORP GEIGY PHARMACEUTICALS DIV

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 200.000 MILLIGRAMS THEOPHYLLINE ACTIVE INGREDIENT
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: LONG ACTION METHOD:EXTENDED RELEASE;
THERAPEUTIC EQUIVALENT: GEIGY

ANGIOVIST 370

DIATRIZOATE MEGLUMINE AND DIATRIZOATE SODIUM INJECTION,USP

NSN, MFG P/N

6505012154392

NSN

6505-01-215-4392

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ANGIOVIST 370

DIATRIZOATE MEGLUMINE AND DIATRIZOATE SODIUM INJECTION,USP

NSN, MFG P/N

6505012154392

NSN

6505-01-215-4392

MFG

BAYER HEALTHCARE PHARMACEUTICALS INC. DBA BERLICHEM

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 10.000 PERCENTAGE, W/V DIATRIZOATE SODIUM ACTIVE INGREDIENT AND 66.000 PERCENTAGE, W/V MEGLUMINE DIATRIZOATE ACTIVE INGREDIENT
III SUPPLEMENTARY FEATURES: MEDSEP ITEM FOR DOD,BERLEX LABS
PRIMARY CONTAINER CONTENT QUANTITY: 50.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL
TOTAL PRIMARY CONTAINER QUANTITY: 50

NDC50419-0190-50

DIATRIZOATE MEGLUMINE AND DIATRIZOATE SODIUM INJECTION,USP

NSN, MFG P/N

6505012154392

NSN

6505-01-215-4392

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NDC50419-0190-50

DIATRIZOATE MEGLUMINE AND DIATRIZOATE SODIUM INJECTION,USP

NSN, MFG P/N

6505012154392

NSN

6505-01-215-4392

MFG

BAYER HEALTHCARE PHARMACEUTICALS INC. DBA BERLICHEM

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 10.000 PERCENTAGE, W/V DIATRIZOATE SODIUM ACTIVE INGREDIENT AND 66.000 PERCENTAGE, W/V MEGLUMINE DIATRIZOATE ACTIVE INGREDIENT
III SUPPLEMENTARY FEATURES: MEDSEP ITEM FOR DOD,BERLEX LABS
PRIMARY CONTAINER CONTENT QUANTITY: 50.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL
TOTAL PRIMARY CONTAINER QUANTITY: 50

HI-210

INSULIN HUMAN INJECTION,USP

NSN, MFG P/N

6505012154825

NSN

6505-01-215-4825

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HI-210

INSULIN HUMAN INJECTION,USP

NSN, MFG P/N

6505012154825

NSN

6505-01-215-4825

MFG

ELI LILLY AND COMPANY DBA ELI LILLY

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 100.000 UNITS INSULIN PER ML. ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: INSULIN HUMAN INJECTION MODIFIED 100UN/ML VIAL
III PROTECTIVE STORAGE FEATURE: SUBJECT TO DAMAGE BY FREEZING AND REQUIRES REFRIGERATION STORAGE BETWEEN 2 TO 8 DEG CELSIUS
III THERAPEUTIC EQUIVALENT: HUMULIN R BY LILLY
PRIMARY CONTAINER CONTENT QUANTITY: 10.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL
SPECIAL FEATURES: MULTIPLE-DOSE VIAL; RECOMBINANT DNA ORIGIN (E. COLI BACTERIA)

HUMULIN-R

INSULIN HUMAN INJECTION,USP

NSN, MFG P/N

6505012154825

NSN

6505-01-215-4825

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HUMULIN-R

INSULIN HUMAN INJECTION,USP

NSN, MFG P/N

6505012154825

NSN

6505-01-215-4825

MFG

ELI LILLY AND COMPANY DBA ELI LILLY

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 100.000 UNITS INSULIN PER ML. ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: INSULIN HUMAN INJECTION MODIFIED 100UN/ML VIAL
III PROTECTIVE STORAGE FEATURE: SUBJECT TO DAMAGE BY FREEZING AND REQUIRES REFRIGERATION STORAGE BETWEEN 2 TO 8 DEG CELSIUS
III THERAPEUTIC EQUIVALENT: HUMULIN R BY LILLY
PRIMARY CONTAINER CONTENT QUANTITY: 10.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL
SPECIAL FEATURES: MULTIPLE-DOSE VIAL; RECOMBINANT DNA ORIGIN (E. COLI BACTERIA)

NDC00002-8215-01

INSULIN HUMAN INJECTION,USP

NSN, MFG P/N

6505012154825

NSN

6505-01-215-4825

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NDC00002-8215-01

INSULIN HUMAN INJECTION,USP

NSN, MFG P/N

6505012154825

NSN

6505-01-215-4825

MFG

ELI LILLY AND COMPANY DBA ELI LILLY

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 100.000 UNITS INSULIN PER ML. ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: INSULIN HUMAN INJECTION MODIFIED 100UN/ML VIAL
III PROTECTIVE STORAGE FEATURE: SUBJECT TO DAMAGE BY FREEZING AND REQUIRES REFRIGERATION STORAGE BETWEEN 2 TO 8 DEG CELSIUS
III THERAPEUTIC EQUIVALENT: HUMULIN R BY LILLY
PRIMARY CONTAINER CONTENT QUANTITY: 10.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL
SPECIAL FEATURES: MULTIPLE-DOSE VIAL; RECOMBINANT DNA ORIGIN (E. COLI BACTERIA)

NDC00169-1833-11

INSULIN HUMAN INJECTION,USP

NSN, MFG P/N

6505012154825

NSN

6505-01-215-4825

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NDC00169-1833-11

INSULIN HUMAN INJECTION,USP

NSN, MFG P/N

6505012154825

NSN

6505-01-215-4825

MFG

NOVO NORDISK INC.

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 100.000 UNITS INSULIN PER ML. ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: INSULIN HUMAN INJECTION MODIFIED 100UN/ML VIAL
III PROTECTIVE STORAGE FEATURE: SUBJECT TO DAMAGE BY FREEZING AND REQUIRES REFRIGERATION STORAGE BETWEEN 2 TO 8 DEG CELSIUS
III THERAPEUTIC EQUIVALENT: HUMULIN R BY LILLY
PRIMARY CONTAINER CONTENT QUANTITY: 10.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL
SPECIAL FEATURES: MULTIPLE-DOSE VIAL; RECOMBINANT DNA ORIGIN (E. COLI BACTERIA)

1505

MAGNESIUM CITRATE ORAL SOLUTION,USP

NSN, MFG P/N

6505012157633

NSN

6505-01-215-7633

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1505

MAGNESIUM CITRATE ORAL SOLUTION,USP

NSN, MFG P/N

6505012157633

NSN

6505-01-215-7633

MFG

NATIONAL MAGNESIA CO INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 10.000 OUNCES MAGNESIUM CITRATE ACTIVE INGREDIENT
FLAVOR: LEMON
PRIMARY CONTAINER CONTENT QUANTITY: 10.000 OUNCES
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: LOW SODIUM

NDC00897-1505-20

MAGNESIUM CITRATE ORAL SOLUTION,USP

NSN, MFG P/N

6505012157633

NSN

6505-01-215-7633

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NDC00897-1505-20

MAGNESIUM CITRATE ORAL SOLUTION,USP

NSN, MFG P/N

6505012157633

NSN

6505-01-215-7633

MFG

NATIONAL MAGNESIA CO INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 10.000 OUNCES MAGNESIUM CITRATE ACTIVE INGREDIENT
FLAVOR: LEMON
PRIMARY CONTAINER CONTENT QUANTITY: 10.000 OUNCES
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: LOW SODIUM

NDC00472-1738-03

MICONAZOLE NITRATE VAGINAL SUPPOSITORIES,USP

NSN, MFG P/N

6505012157753

NSN

6505-01-215-7753

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NDC00472-1738-03

MICONAZOLE NITRATE VAGINAL SUPPOSITORIES,USP

NSN, MFG P/N

6505012157753

NSN

6505-01-215-7753

MFG

DIXON-SHANE LLC DBA R & S NORTHEAST

Description

ACTIVE INGREDIENT AND STRENGTH: 200.000 MICONAZOLE NITRATE MILLIGRAMS
FEATURES PROVIDED: INDIVIDUALLY SEALED
III PART NAME ASSIGNED BY CONTROLLING AGENCY: MICONAZOLE NITRATE VAGINAL SUPPOSITORIES USP 200MG I.S. 3S
PRIMARY CONTAINER TYPE: PACKAGE
SPECIAL FEATURES: SUPPOSITORIES PACKAGED WITH VAGINAL APPLICATOR
SUPPLEMENTARY FEATURES: D-DAY ITEM FOR DOD
SUPPOSITORY TYPE: VAGINAL

NDC55390-0103-10

ATRACURIUM BESYLATE INJECTION

NSN, MFG P/N

6505012157755

NSN

6505-01-215-7755

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NDC55390-0103-10

ATRACURIUM BESYLATE INJECTION

NSN, MFG P/N

6505012157755

NSN

6505-01-215-7755

MFG

CARDINAL HEALTH INC. DBA CARDINAL HEALTH

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 10.000 MILLIGRAMS ATRACURIUM BESYLATE PER MILLILITER
III PART NAME ASSIGNED BY CONTROLLING AGENCY: ATRACURIUM BESYLATE INJECTION 10MG/ML 10ML VIAL 10S
PRIMARY CONTAINER CONTENT QUANTITY: 10.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL
SPECIAL FEATURES: MULTIDOSE VIALS
TOTAL PRIMARY CONTAINER QUANTITY: 10

NDC61703-0313-32

ATRACURIUM BESYLATE INJECTION

NSN, MFG P/N

6505012157755

NSN

6505-01-215-7755

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NDC61703-0313-32

ATRACURIUM BESYLATE INJECTION

NSN, MFG P/N

6505012157755

NSN

6505-01-215-7755

MFG

FAULDING PHARMACEUTICALS

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 10.000 MILLIGRAMS ATRACURIUM BESYLATE PER MILLILITER
III PART NAME ASSIGNED BY CONTROLLING AGENCY: ATRACURIUM BESYLATE INJECTION 10MG/ML 10ML VIAL 10S
PRIMARY CONTAINER CONTENT QUANTITY: 10.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL
SPECIAL FEATURES: MULTIDOSE VIALS
TOTAL PRIMARY CONTAINER QUANTITY: 10

NDC00182-0183-10

PREDNISOLONE TABLETS,USP

NSN, MFG P/N

6505012158102

NSN

6505-01-215-8102

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NDC00182-0183-10

PREDNISOLONE TABLETS,USP

NSN, MFG P/N

6505012158102

NSN

6505-01-215-8102

MFG

GOLDLINE LABORATORIES INC. DBA GOLDLINE LABORATORIES

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 5.000 MILLIGRAMS PREDNISOLONE ACTIVE INGREDIENT
PRIMARY CONTAINER CONTENT QUANTITY: 1000.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

ANGIOVIST 370

DIATRIZOATE MEGLUMINE AND DIATRIZOATE SODIUM INJECTION,USP

NSN, MFG P/N

6505012158103

NSN

6505-01-215-8103

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ANGIOVIST 370

DIATRIZOATE MEGLUMINE AND DIATRIZOATE SODIUM INJECTION,USP

NSN, MFG P/N

6505012158103

NSN

6505-01-215-8103

MFG

BAYER HEALTHCARE PHARMACEUTICALS INC. DBA BERLICHEM

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 10.000 PERCENTAGE, W/V P-DITOLYMERCURY ACTIVE INGREDIENT AND DIATRIZOATE MEGLUMINE 66% V/W ACTIVE INGREDIENT
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL
TOTAL PRIMARY CONTAINER QUANTITY: 20