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6505-01-367-5510

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AC-1016

HEMODIALYSIS SOLUTION,CONCENTRATED

NSN, MFG P/N

6505013675510

NSN

6505-01-367-5510

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AC-1016

HEMODIALYSIS SOLUTION,CONCENTRATED

NSN, MFG P/N

6505013675510

NSN

6505-01-367-5510

MFG

U S DEPT OF VETERANS AFFAIRS

Description

PRIMARY CONTAINER CONTENT QUANTITY: 128.000 FLUID OUNCES
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: 6 GALLONS PER PACKAGE

PRELONE

PREDNISOLONE ORAL SOLUTION

NSN, MFG P/N

6505013671081

NSN

6505-01-367-1081

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PRELONE

PREDNISOLONE ORAL SOLUTION

NSN, MFG P/N

6505013671081

NSN

6505-01-367-1081

MFG

AERO PHARMACEUTICALS INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 15.000 MILLILITERS PREDNISOLONE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: PREDNISOLONE ORAL SOLUTION CHERRY FLAVORED 15MG/5ML 240ML BT
PRIMARY CONTAINER CONTENT QUANTITY: 240.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: CHERRY FLAVORED,W/5 PCT ALCOHOL

NDC00409-1966-07

SODIUM CHLORIDE INJECTION,BACTERIOSTATIC,USP

NSN, MFG P/N

6505013674584

NSN

6505-01-367-4584

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NDC00409-1966-07

SODIUM CHLORIDE INJECTION,BACTERIOSTATIC,USP

NSN, MFG P/N

6505013674584

NSN

6505-01-367-4584

MFG

HOSPIRA INC.

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 0.900 PERCENTAGE, W/V SODIUM CHLORIDE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: SODIUM CHLORIDE INJECTION BACTERIOSTATIC USP 30ML VIAL 25S
III PROTECTIVE STORAGE FEATURE: EXPIRATION DATED
PHARMACEUTICAL VEHICLE TYPE: AQUEOUS
PRIMARY CONTAINER CONTENT QUANTITY: 30.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL, MULTIPLE DOSE
SPECIAL FEATURES: PRESERVED WITH 0.9% BENZYL ALCOHOL
TOTAL PRIMARY CONTAINER QUANTITY: 25

NDC63323-0924-30

SODIUM CHLORIDE INJECTION,BACTERIOSTATIC,USP

NSN, MFG P/N

6505013674584

NSN

6505-01-367-4584

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NDC63323-0924-30

SODIUM CHLORIDE INJECTION,BACTERIOSTATIC,USP

NSN, MFG P/N

6505013674584

NSN

6505-01-367-4584

MFG

AMERICAN PHARMACEUTICAL PARTNERS

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 0.900 PERCENTAGE, W/V SODIUM CHLORIDE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: SODIUM CHLORIDE INJECTION BACTERIOSTATIC USP 30ML VIAL 25S
III PROTECTIVE STORAGE FEATURE: EXPIRATION DATED
PHARMACEUTICAL VEHICLE TYPE: AQUEOUS
PRIMARY CONTAINER CONTENT QUANTITY: 30.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL, MULTIPLE DOSE
SPECIAL FEATURES: PRESERVED WITH 0.9% BENZYL ALCOHOL
TOTAL PRIMARY CONTAINER QUANTITY: 25

CALPHOSAN

CALCIUM LACTATE AND

NSN, MFG P/N

6505013675224

NSN

6505-01-367-5224

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CALPHOSAN

CALCIUM LACTATE AND

NSN, MFG P/N

6505013675224

NSN

6505-01-367-5224

MFG

GLENWOOD LLC

Description

GENERAL CHARACTERISTICS ITEM DESCRIPTION: 50 MG CALCIUM LACTATE AND 50 MG CALCIUM GLYCERPHOSPHATE PER 10 ML; 60 ML PER MULTIDOSE VIAL
III PART NAME ASSIGNED BY CONTROLLING AGENCY: CALCIUM LACTATE AND CALCIUM GYLCERPHOSPHATE INJECTION 60ML VIAL

F92I227

CALCIUM LACTATE AND

NSN, MFG P/N

6505013675224

NSN

6505-01-367-5224

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F92I227

CALCIUM LACTATE AND

NSN, MFG P/N

6505013675224

NSN

6505-01-367-5224

MFG

AIR FORCE MEDICAL LOGISTICS OFFICE

Description

GENERAL CHARACTERISTICS ITEM DESCRIPTION: 50 MG CALCIUM LACTATE AND 50 MG CALCIUM GLYCERPHOSPHATE PER 10 ML; 60 ML PER MULTIDOSE VIAL
III PART NAME ASSIGNED BY CONTROLLING AGENCY: CALCIUM LACTATE AND CALCIUM GYLCERPHOSPHATE INJECTION 60ML VIAL

NDC00516-0060-60

CALCIUM LACTATE AND

NSN, MFG P/N

6505013675224

NSN

6505-01-367-5224

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NDC00516-0060-60

CALCIUM LACTATE AND

NSN, MFG P/N

6505013675224

NSN

6505-01-367-5224

MFG

GLENWOOD LLC

Description

GENERAL CHARACTERISTICS ITEM DESCRIPTION: 50 MG CALCIUM LACTATE AND 50 MG CALCIUM GLYCERPHOSPHATE PER 10 ML; 60 ML PER MULTIDOSE VIAL
III PART NAME ASSIGNED BY CONTROLLING AGENCY: CALCIUM LACTATE AND CALCIUM GYLCERPHOSPHATE INJECTION 60ML VIAL

NDC00069-1520-68

AMLODIPINE BESYLATE TABLETS

NSN, MFG P/N

6505013675242

NSN

6505-01-367-5242

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NDC00069-1520-68

AMLODIPINE BESYLATE TABLETS

NSN, MFG P/N

6505013675242

NSN

6505-01-367-5242

MFG

PFIZER INC. DBA PFIZER

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 2.500 MILLIGRAMS AMLODIPINE BESYLATE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: AMLODIPINE BESYLATE TABLETS 2.5MG 90S BT
PRIMARY CONTAINER CONTENT QUANTITY: 90.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

NORVASC

AMLODIPINE BESYLATE TABLETS

NSN, MFG P/N

6505013675242

NSN

6505-01-367-5242

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NORVASC

AMLODIPINE BESYLATE TABLETS

NSN, MFG P/N

6505013675242

NSN

6505-01-367-5242

MFG

PFIZER INC. DBA PFIZER

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 2.500 MILLIGRAMS AMLODIPINE BESYLATE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: AMLODIPINE BESYLATE TABLETS 2.5MG 90S BT
PRIMARY CONTAINER CONTENT QUANTITY: 90.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

NDC00069-1540-68

AMLODIPINE BESYLATE TABLETS

NSN, MFG P/N

6505013675243

NSN

6505-01-367-5243

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NDC00069-1540-68

AMLODIPINE BESYLATE TABLETS

NSN, MFG P/N

6505013675243

NSN

6505-01-367-5243

MFG

PFIZER INC. DBA PFIZER

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 10.000 MILLIGRAMS AMLODIPINE BESYLATE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: AMLODIPINE BESYLATE TABLETS 10MG 90S BT
PRIMARY CONTAINER CONTENT QUANTITY: 90.000 TABLETS
PRIMARY CONTAINER TYPE: PACKAGE

NORVASC

AMLODIPINE BESYLATE TABLETS

NSN, MFG P/N

6505013675243

NSN

6505-01-367-5243

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NORVASC

AMLODIPINE BESYLATE TABLETS

NSN, MFG P/N

6505013675243

NSN

6505-01-367-5243

MFG

PFIZER INC. DBA PFIZER

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 10.000 MILLIGRAMS AMLODIPINE BESYLATE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: AMLODIPINE BESYLATE TABLETS 10MG 90S BT
PRIMARY CONTAINER CONTENT QUANTITY: 90.000 TABLETS
PRIMARY CONTAINER TYPE: PACKAGE

NDC00069-1530-68

AMLODIPINE BESYLATE TABLETS

NSN, MFG P/N

6505013675244

NSN

6505-01-367-5244

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NDC00069-1530-68

AMLODIPINE BESYLATE TABLETS

NSN, MFG P/N

6505013675244

NSN

6505-01-367-5244

MFG

PFIZER INC. DBA PFIZER

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 5.000 MILLIGRAMS AMLODIPINE BESYLATE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: AMLODIPINE BESYLATE TABLETS 5MG 90S BT
PRIMARY CONTAINER CONTENT QUANTITY: 90.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

NDC59762-1530-01

AMLODIPINE BESYLATE TABLETS

NSN, MFG P/N

6505013675244

NSN

6505-01-367-5244

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NDC59762-1530-01

AMLODIPINE BESYLATE TABLETS

NSN, MFG P/N

6505013675244

NSN

6505-01-367-5244

MFG

DIXON-SHANE LLC DBA R & S NORTHEAST

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 5.000 MILLIGRAMS AMLODIPINE BESYLATE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: AMLODIPINE BESYLATE TABLETS 5MG 90S BT
PRIMARY CONTAINER CONTENT QUANTITY: 90.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

NORVASC

AMLODIPINE BESYLATE TABLETS

NSN, MFG P/N

6505013675244

NSN

6505-01-367-5244

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NORVASC

AMLODIPINE BESYLATE TABLETS

NSN, MFG P/N

6505013675244

NSN

6505-01-367-5244

MFG

PFIZER INC. DBA PFIZER

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 5.000 MILLIGRAMS AMLODIPINE BESYLATE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: AMLODIPINE BESYLATE TABLETS 5MG 90S BT
PRIMARY CONTAINER CONTENT QUANTITY: 90.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

F92G223

INTERFERON ALFA-N3

NSN, MFG P/N

6505013675248

NSN

6505-01-367-5248

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F92G223

INTERFERON ALFA-N3

NSN, MFG P/N

6505013675248

NSN

6505-01-367-5248

MFG

AIR FORCE MEDICAL LOGISTICS OFFICE

Description

GENERAL CHARACTERISTICS ITEM DESCRIPTION: CONTAINS 5000000 INTERNATIONAL UNITS INTERFERON ALFA-N3 PER ML; INTRALESIONAL; MULTI DOSE VIAL,STERILE; NOT RECOMBINANT; 1 ML REQUIRES REFRIGERATION; 12 PER PACKAGE; ANTINEOPLASTIC DRUG
III PART NAME ASSIGNED BY CONTROLLING AGENCY: INTERFERON ALFA-N3 INJECSTION 5000000 I.U./ML 12S

NDC54746-0001-01

INTERFERON ALFA-N3

NSN, MFG P/N

6505013675248

NSN

6505-01-367-5248

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NDC54746-0001-01

INTERFERON ALFA-N3

NSN, MFG P/N

6505013675248

NSN

6505-01-367-5248

MFG

DEFENSE LOGISTICS AGENCY DIRECTORATE OF MEDICAL MATERIEL DEFENSE SUPPLY CENTER PHILADELPHIA

Description

GENERAL CHARACTERISTICS ITEM DESCRIPTION: CONTAINS 5000000 INTERNATIONAL UNITS INTERFERON ALFA-N3 PER ML; INTRALESIONAL; MULTI DOSE VIAL,STERILE; NOT RECOMBINANT; 1 ML REQUIRES REFRIGERATION; 12 PER PACKAGE; ANTINEOPLASTIC DRUG
III PART NAME ASSIGNED BY CONTROLLING AGENCY: INTERFERON ALFA-N3 INJECSTION 5000000 I.U./ML 12S

KETALAR

KETAMINE HYDROCHLORIDE INJECTION,USP

NSN, MFG P/N

6505013675261

NSN

6505-01-367-5261

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KETALAR

KETAMINE HYDROCHLORIDE INJECTION,USP

NSN, MFG P/N

6505013675261

NSN

6505-01-367-5261

MFG

PARKE-DAVIS DIV OF WARNER-LAMBERT CO

Description

III PART NAME ASSIGNED BY CONTROLLING AGENCY: KETAMINE HYDROCHLORIDE INJECTION USP 20ML VIAL 10S
III PROTECTIVE STORAGE FEATURE: SUBJECT TO DAMAGE BY FREEZING
PRIMARY CONTAINER CONTENT QUANTITY: 20.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL
SPECIAL FEATURES: EQUIVALENT TO 10 MG KETAMINE PER ML
TOTAL PRIMARY CONTAINER QUANTITY: 10

NDC42023-0113-10

KETAMINE HYDROCHLORIDE INJECTION,USP

NSN, MFG P/N

6505013675261

NSN

6505-01-367-5261

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NDC42023-0113-10

KETAMINE HYDROCHLORIDE INJECTION,USP

NSN, MFG P/N

6505013675261

NSN

6505-01-367-5261

MFG

MONARCH PHARMACEUTICALS INC

Description

III PART NAME ASSIGNED BY CONTROLLING AGENCY: KETAMINE HYDROCHLORIDE INJECTION USP 20ML VIAL 10S
III PROTECTIVE STORAGE FEATURE: SUBJECT TO DAMAGE BY FREEZING
PRIMARY CONTAINER CONTENT QUANTITY: 20.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL
SPECIAL FEATURES: EQUIVALENT TO 10 MG KETAMINE PER ML
TOTAL PRIMARY CONTAINER QUANTITY: 10

AQUASOL E

VITAMIN E ORAL SOLUTION

NSN, MFG P/N

6505013675262

NSN

6505-01-367-5262

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AQUASOL E

VITAMIN E ORAL SOLUTION

NSN, MFG P/N

6505013675262

NSN

6505-01-367-5262

MFG

ASTRA PHARMACEUTICALS LP

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 50.000 INTERNATIONAL UNITS DL-ALPHA-TOCOPHERYL ACETATE PER MILLILITER
III PART NAME ASSIGNED BY CONTROLLING AGENCY: VITAMIN E ORAL SOLUTION 30ML BT
PRIMARY CONTAINER CONTENT QUANTITY: 30.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE, DROPPER
SPECIAL FEATURES: W/SCREW-CAP CLOSURE AND CALIBRATED DROPPER

NDC00186-5800-30

VITAMIN E ORAL SOLUTION

NSN, MFG P/N

6505013675262

NSN

6505-01-367-5262

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NDC00186-5800-30

VITAMIN E ORAL SOLUTION

NSN, MFG P/N

6505013675262

NSN

6505-01-367-5262

MFG

ASTRA PHARMACEUTICALS LP

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 50.000 INTERNATIONAL UNITS DL-ALPHA-TOCOPHERYL ACETATE PER MILLILITER
III PART NAME ASSIGNED BY CONTROLLING AGENCY: VITAMIN E ORAL SOLUTION 30ML BT
PRIMARY CONTAINER CONTENT QUANTITY: 30.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE, DROPPER
SPECIAL FEATURES: W/SCREW-CAP CLOSURE AND CALIBRATED DROPPER