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6505-01-293-5580

20 Products

ZILACTIN GEL

TANNIC ACID GEL

NSN, MFG P/N

6505012935580

NSN

6505-01-293-5580

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ZILACTIN GEL

TANNIC ACID GEL

NSN, MFG P/N

6505012935580

NSN

6505-01-293-5580

MFG

ZILA PHARMACEUTICALS INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 7.000 PERCENTAGE, W/V TANNIC ACID ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: TANNIC ACID GEL 7% 0.25OZ TUBE
III SUPPLEMENTARY FEATURES: MEDSEP ITEM FOR DOD,ZILA PHARMACEUTICALS INC
PRIMARY CONTAINER CONTENT QUANTITY: 0.250 OUNCES
PRIMARY CONTAINER TYPE: TUBE
SPECIAL FEATURES: USE PREFERRED UPC: 3-50486-46802-4 IN ACCORDANCE WITH THE JDF

NDC00065-0259-15

HYDROXYETHYLCELLULO

NSN, MFG P/N

6505012929823

NSN

6505-01-292-9823

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NDC00065-0259-15

HYDROXYETHYLCELLULO

NSN, MFG P/N

6505012929823

NSN

6505-01-292-9823

MFG

ALCON LABORATORIES INC .

Description

GENERAL CHARACTERISTICS ITEM DESCRIPTION: .5 PCT. W/V HYDROXYETHYLCELLULOSE EQUIVALENT; STERILE; BUFFERED; ISOTONIC; 15 ML BOTTLE WITH OPHTHALMIC TIP; SQUEEZE BOTTLE; PROVIDES A REFRACTIVE INDEX OF APPROXIMATELY 1.35; FOR BONDING GONIOSCOPIC PRISM TO THE EYE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: HYDROXYETHYLCELLULOSE OPHTHALMIC SOLUTION 0.5% 15ML BT

ACCUTANE

ISOTRETINOIN CAPSULES,USP

NSN, MFG P/N

6505012929831

NSN

6505-01-292-9831

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ACCUTANE

ISOTRETINOIN CAPSULES,USP

NSN, MFG P/N

6505012929831

NSN

6505-01-292-9831

MFG

ROCHE LABORATORIES INC.

Description

(NON-CORE DATA) EXTERIOR CONTAINER CUBIC MEASURE: 0.06 CUBIC FEET
(NON-CORE DATA) EXTERIOR CONTAINER QUANTITY: 6
(NON-CORE DATA) EXTERIOR CONTAINER WEIGHT: 2.00 POUNDS
(NON-CORE DATA) UNIT OF ISSUE CUBE: 0.01 CUBIC FEET
(NON-CORE DATA) UNIT OF ISSUE WEIGHT: 0.30 POUNDS
(NON-CORE DATA) UNIT PACKAGE TYPE: PACKAGE
ACTIVE MEDICAMENT MEDICINAL STRENGTH: 10.000 MILLIGRAMS ISOTRETINOIN ACTIVE INGREDIENT
CAPSULE CONTENT FORM: ANY ACCEPTABLE
CAPSULE PRIMARY CONTAINER CONTENT QUANTITY: 100.000
CAPSULE TYPE: ANY ACCEPTABLE
FEATURES PROVIDED: INDIVIDUALLY SEALED
III PART NAME ASSIGNED BY CONTROLLING AGENCY: ISOTRETINOIN CAPSULES 10MG I.S. 100S PG
PRIMARY CONTAINER TYPE: STRIP

ACCUTANE CAPSULES

ISOTRETINOIN CAPSULES,USP

NSN, MFG P/N

6505012929831

NSN

6505-01-292-9831

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ACCUTANE CAPSULES

ISOTRETINOIN CAPSULES,USP

NSN, MFG P/N

6505012929831

NSN

6505-01-292-9831

MFG

ROCHE LABORATORIES INC.

Description

(NON-CORE DATA) EXTERIOR CONTAINER CUBIC MEASURE: 0.06 CUBIC FEET
(NON-CORE DATA) EXTERIOR CONTAINER QUANTITY: 6
(NON-CORE DATA) EXTERIOR CONTAINER WEIGHT: 2.00 POUNDS
(NON-CORE DATA) UNIT OF ISSUE CUBE: 0.01 CUBIC FEET
(NON-CORE DATA) UNIT OF ISSUE WEIGHT: 0.30 POUNDS
(NON-CORE DATA) UNIT PACKAGE TYPE: PACKAGE
ACTIVE MEDICAMENT MEDICINAL STRENGTH: 10.000 MILLIGRAMS ISOTRETINOIN ACTIVE INGREDIENT
CAPSULE CONTENT FORM: ANY ACCEPTABLE
CAPSULE PRIMARY CONTAINER CONTENT QUANTITY: 100.000
CAPSULE TYPE: ANY ACCEPTABLE
FEATURES PROVIDED: INDIVIDUALLY SEALED
III PART NAME ASSIGNED BY CONTROLLING AGENCY: ISOTRETINOIN CAPSULES 10MG I.S. 100S PG
PRIMARY CONTAINER TYPE: STRIP

NDC00004-0155-49

ISOTRETINOIN CAPSULES,USP

NSN, MFG P/N

6505012929831

NSN

6505-01-292-9831

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NDC00004-0155-49

ISOTRETINOIN CAPSULES,USP

NSN, MFG P/N

6505012929831

NSN

6505-01-292-9831

MFG

ROCHE LABORATORIES INC.

Description

(NON-CORE DATA) EXTERIOR CONTAINER CUBIC MEASURE: 0.06 CUBIC FEET
(NON-CORE DATA) EXTERIOR CONTAINER QUANTITY: 6
(NON-CORE DATA) EXTERIOR CONTAINER WEIGHT: 2.00 POUNDS
(NON-CORE DATA) UNIT OF ISSUE CUBE: 0.01 CUBIC FEET
(NON-CORE DATA) UNIT OF ISSUE WEIGHT: 0.30 POUNDS
(NON-CORE DATA) UNIT PACKAGE TYPE: PACKAGE
ACTIVE MEDICAMENT MEDICINAL STRENGTH: 10.000 MILLIGRAMS ISOTRETINOIN ACTIVE INGREDIENT
CAPSULE CONTENT FORM: ANY ACCEPTABLE
CAPSULE PRIMARY CONTAINER CONTENT QUANTITY: 100.000
CAPSULE TYPE: ANY ACCEPTABLE
FEATURES PROVIDED: INDIVIDUALLY SEALED
III PART NAME ASSIGNED BY CONTROLLING AGENCY: ISOTRETINOIN CAPSULES 10MG I.S. 100S PG
PRIMARY CONTAINER TYPE: STRIP

ACCUTANE

ISOTRETINOIN CAPSULES,USP

NSN, MFG P/N

6505012929832

NSN

6505-01-292-9832

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ACCUTANE

ISOTRETINOIN CAPSULES,USP

NSN, MFG P/N

6505012929832

NSN

6505-01-292-9832

MFG

ROCHE LABORATORIES INC.

Description

(NON-CORE DATA) EXTERIOR CONTAINER CUBIC MEASURE: 0.06 CUBIC FEET
(NON-CORE DATA) EXTERIOR CONTAINER QUANTITY: 6
(NON-CORE DATA) EXTERIOR CONTAINER WEIGHT: 2.00 POUNDS
(NON-CORE DATA) UNIT OF ISSUE CUBE: 0.01 CUBIC FEET
(NON-CORE DATA) UNIT OF ISSUE WEIGHT: 0.30 POUNDS
(NON-CORE DATA) UNIT PACKAGE TYPE: PACKAGE
ACTIVE MEDICAMENT MEDICINAL STRENGTH: 40.000 MILLIGRAMS ISOTRETINOIN ACTIVE INGREDIENT
CAPSULE CONTENT FORM: ANY ACCEPTABLE
CAPSULE PRIMARY CONTAINER CONTENT QUANTITY: 100.000
CAPSULE TYPE: ANY ACCEPTABLE
FEATURES PROVIDED: INDIVIDUALLY SEALED
III PART NAME ASSIGNED BY CONTROLLING AGENCY: ISOTRETINOIN CAPSULES 40MG I.S. 100S PG
PRIMARY CONTAINER TYPE: STRIP

ACCUTANE CAPSULES

ISOTRETINOIN CAPSULES,USP

NSN, MFG P/N

6505012929832

NSN

6505-01-292-9832

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ACCUTANE CAPSULES

ISOTRETINOIN CAPSULES,USP

NSN, MFG P/N

6505012929832

NSN

6505-01-292-9832

MFG

ROCHE LABORATORIES INC.

Description

(NON-CORE DATA) EXTERIOR CONTAINER CUBIC MEASURE: 0.06 CUBIC FEET
(NON-CORE DATA) EXTERIOR CONTAINER QUANTITY: 6
(NON-CORE DATA) EXTERIOR CONTAINER WEIGHT: 2.00 POUNDS
(NON-CORE DATA) UNIT OF ISSUE CUBE: 0.01 CUBIC FEET
(NON-CORE DATA) UNIT OF ISSUE WEIGHT: 0.30 POUNDS
(NON-CORE DATA) UNIT PACKAGE TYPE: PACKAGE
ACTIVE MEDICAMENT MEDICINAL STRENGTH: 40.000 MILLIGRAMS ISOTRETINOIN ACTIVE INGREDIENT
CAPSULE CONTENT FORM: ANY ACCEPTABLE
CAPSULE PRIMARY CONTAINER CONTENT QUANTITY: 100.000
CAPSULE TYPE: ANY ACCEPTABLE
FEATURES PROVIDED: INDIVIDUALLY SEALED
III PART NAME ASSIGNED BY CONTROLLING AGENCY: ISOTRETINOIN CAPSULES 40MG I.S. 100S PG
PRIMARY CONTAINER TYPE: STRIP

NDC00004-0156-49

ISOTRETINOIN CAPSULES,USP

NSN, MFG P/N

6505012929832

NSN

6505-01-292-9832

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NDC00004-0156-49

ISOTRETINOIN CAPSULES,USP

NSN, MFG P/N

6505012929832

NSN

6505-01-292-9832

MFG

ROCHE LABORATORIES INC.

Description

(NON-CORE DATA) EXTERIOR CONTAINER CUBIC MEASURE: 0.06 CUBIC FEET
(NON-CORE DATA) EXTERIOR CONTAINER QUANTITY: 6
(NON-CORE DATA) EXTERIOR CONTAINER WEIGHT: 2.00 POUNDS
(NON-CORE DATA) UNIT OF ISSUE CUBE: 0.01 CUBIC FEET
(NON-CORE DATA) UNIT OF ISSUE WEIGHT: 0.30 POUNDS
(NON-CORE DATA) UNIT PACKAGE TYPE: PACKAGE
ACTIVE MEDICAMENT MEDICINAL STRENGTH: 40.000 MILLIGRAMS ISOTRETINOIN ACTIVE INGREDIENT
CAPSULE CONTENT FORM: ANY ACCEPTABLE
CAPSULE PRIMARY CONTAINER CONTENT QUANTITY: 100.000
CAPSULE TYPE: ANY ACCEPTABLE
FEATURES PROVIDED: INDIVIDUALLY SEALED
III PART NAME ASSIGNED BY CONTROLLING AGENCY: ISOTRETINOIN CAPSULES 40MG I.S. 100S PG
PRIMARY CONTAINER TYPE: STRIP

NDC00264-1128-50

DEXTROSE INJECTION,USP

NSN, MFG P/N

6505012931338

NSN

6505-01-293-1338

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NDC00264-1128-50

DEXTROSE INJECTION,USP

NSN, MFG P/N

6505012931338

NSN

6505-01-293-1338

MFG

B BRAUN MEDICAL INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 50.000 PERCENTAGE, W/V DEXTROSE ACTIVE INGREDIENT
ADMINISTRATION: INTRAVENOUS
PHARMACEUTICAL VEHICLE TYPE: AQUEOUS
PRIMARY CONTAINER CONTENT QUANTITY: 2000.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE
TOTAL PRIMARY CONTAINER QUANTITY: 6

S1285

DEXTROSE INJECTION,USP

NSN, MFG P/N

6505012931338

NSN

6505-01-293-1338

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S1285

DEXTROSE INJECTION,USP

NSN, MFG P/N

6505012931338

NSN

6505-01-293-1338

MFG

B BRAUN MEDICAL INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 50.000 PERCENTAGE, W/V DEXTROSE ACTIVE INGREDIENT
ADMINISTRATION: INTRAVENOUS
PHARMACEUTICAL VEHICLE TYPE: AQUEOUS
PRIMARY CONTAINER CONTENT QUANTITY: 2000.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE
TOTAL PRIMARY CONTAINER QUANTITY: 6

CREON

PANCRELIPASE CAPSULES,MODIFIED

NSN, MFG P/N

6505012931904

NSN

6505-01-293-1904

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CREON

PANCRELIPASE CAPSULES,MODIFIED

NSN, MFG P/N

6505012931904

NSN

6505-01-293-1904

MFG

REID ROWELL

Description

CAPSULE CONTENT FORM: ANY ACCEPTABLE
CAPSULE PRIMARY CONTAINER CONTENT QUANTITY: 250.000
CAPSULE TYPE: ANY ACCEPTABLE
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: 30,000 USP UNITS AMYLASE,8,000 USP UNITS LIPASE,AND 13,000 USP UNITS PROTEASE

CREON CAPSULES

PANCRELIPASE CAPSULES,MODIFIED

NSN, MFG P/N

6505012931904

NSN

6505-01-293-1904

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CREON CAPSULES

PANCRELIPASE CAPSULES,MODIFIED

NSN, MFG P/N

6505012931904

NSN

6505-01-293-1904

MFG

REID ROWELL

Description

CAPSULE CONTENT FORM: ANY ACCEPTABLE
CAPSULE PRIMARY CONTAINER CONTENT QUANTITY: 250.000
CAPSULE TYPE: ANY ACCEPTABLE
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: 30,000 USP UNITS AMYLASE,8,000 USP UNITS LIPASE,AND 13,000 USP UNITS PROTEASE

NDC00032-1200-07

PANCRELIPASE CAPSULES,MODIFIED

NSN, MFG P/N

6505012931904

NSN

6505-01-293-1904

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NDC00032-1200-07

PANCRELIPASE CAPSULES,MODIFIED

NSN, MFG P/N

6505012931904

NSN

6505-01-293-1904

MFG

REID ROWELL

Description

CAPSULE CONTENT FORM: ANY ACCEPTABLE
CAPSULE PRIMARY CONTAINER CONTENT QUANTITY: 250.000
CAPSULE TYPE: ANY ACCEPTABLE
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: 30,000 USP UNITS AMYLASE,8,000 USP UNITS LIPASE,AND 13,000 USP UNITS PROTEASE

NDC00517-2110-25

POTASSIUM CHLORIDE INJECTION,USP

NSN, MFG P/N

6505012931905

NSN

6505-01-293-1905

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NDC00517-2110-25

POTASSIUM CHLORIDE INJECTION,USP

NSN, MFG P/N

6505012931905

NSN

6505-01-293-1905

MFG

LUITPOLD PHARMACEUTICALS INC OSTEOHEALTH COMPANY OSTEOHEALTH DIV

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 20.000 MILLIEQUIVALENTS POTASSIUM CHLORIDE ACTIVE INGREDIENT
PRIMARY CONTAINER CONTENT QUANTITY: 10.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL, MULTIPLE DOSE
TOTAL PRIMARY CONTAINER QUANTITY: 25
UNIT PACKAGE TYPE: PACKAGE

HYPAQUE-76

DIATRIZOATE MEGLUMINE AND DIATRIZOATE SODIUM INJECTION,USP

NSN, MFG P/N

6505012931906

NSN

6505-01-293-1906

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HYPAQUE-76

DIATRIZOATE MEGLUMINE AND DIATRIZOATE SODIUM INJECTION,USP

NSN, MFG P/N

6505012931906

NSN

6505-01-293-1906

MFG

STERLING-WINTHROP RESEARCH INSTITUTE A DIV OF STERLING DRUG INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 10.000 PERCENTAGE, W/V DIATRIZOATE SODIUM ACTIVE INGREDIENT AND 66.000 PERCENTAGE, W/V MEGLUMINE DIATRIZOATE ACTIVE INGREDIENT
PHARMACEUTICAL VEHICLE TYPE: AQUEOUS
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE
TOTAL PRIMARY CONTAINER QUANTITY: 10

NDC00024-0779-02

DIATRIZOATE MEGLUMINE AND DIATRIZOATE SODIUM INJECTION,USP

NSN, MFG P/N

6505012931906

NSN

6505-01-293-1906

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NDC00024-0779-02

DIATRIZOATE MEGLUMINE AND DIATRIZOATE SODIUM INJECTION,USP

NSN, MFG P/N

6505012931906

NSN

6505-01-293-1906

MFG

STERLING-WINTHROP RESEARCH INSTITUTE A DIV OF STERLING DRUG INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 10.000 PERCENTAGE, W/V DIATRIZOATE SODIUM ACTIVE INGREDIENT AND 66.000 PERCENTAGE, W/V MEGLUMINE DIATRIZOATE ACTIVE INGREDIENT
PHARMACEUTICAL VEHICLE TYPE: AQUEOUS
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE
TOTAL PRIMARY CONTAINER QUANTITY: 10

CLEOCIN ADDVANTAGE

CLINDAMYCIN INJECTION,USP

NSN, MFG P/N

6505012933319

NSN

6505-01-293-3319

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CLEOCIN ADDVANTAGE

CLINDAMYCIN INJECTION,USP

NSN, MFG P/N

6505012933319

NSN

6505-01-293-3319

MFG

PHARMACIA & UPJOHN COMPANY

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 150.000 MILLIGRAMS CLINDAMYCIN EQUIVALENT PER MILLILITER
ADMINISTRATION: INTRAVENOUS
FEATURES PROVIDED: STERILE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: CLINDAMYCIN INJECTION USP STERILE 150MG/ML 4ML VIAL 25S
PRIMARY CONTAINER CONTENT QUANTITY: 4.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL, SINGLE DOSE
SPECIAL FEATURES: 600 MG IN A SINGLE-DOSE,15 ML CAPACITY GLASS VIAL W/DOUBLED LEAD SCREW TO INTERLOCK W/INLET PORT OF DEXTROSE INJECTION,6505-01-260-1237,6505-01-260-1238,6505-01-260-1239 AND SODIUM CHLORIDE INJECTION,6505-01-260-1241,6505-01-260-1242,AND 6505-01-260-6715;
TOTAL PRIMARY CONTAINER QUANTITY: 25
~1: EACH DRUG VIAL SHALL BE ENCLOSED IN AN UPPER AND LOWER PLASTIC SHROUD

CLEOCIN PHOSPHAT

CLINDAMYCIN INJECTION,USP

NSN, MFG P/N

6505012933319

NSN

6505-01-293-3319

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CLEOCIN PHOSPHAT

CLINDAMYCIN INJECTION,USP

NSN, MFG P/N

6505012933319

NSN

6505-01-293-3319

MFG

PHARMACIA & UPJOHN COMPANY

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 150.000 MILLIGRAMS CLINDAMYCIN EQUIVALENT PER MILLILITER
ADMINISTRATION: INTRAVENOUS
FEATURES PROVIDED: STERILE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: CLINDAMYCIN INJECTION USP STERILE 150MG/ML 4ML VIAL 25S
PRIMARY CONTAINER CONTENT QUANTITY: 4.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL, SINGLE DOSE
SPECIAL FEATURES: 600 MG IN A SINGLE-DOSE,15 ML CAPACITY GLASS VIAL W/DOUBLED LEAD SCREW TO INTERLOCK W/INLET PORT OF DEXTROSE INJECTION,6505-01-260-1237,6505-01-260-1238,6505-01-260-1239 AND SODIUM CHLORIDE INJECTION,6505-01-260-1241,6505-01-260-1242,AND 6505-01-260-6715;
TOTAL PRIMARY CONTAINER QUANTITY: 25
~1: EACH DRUG VIAL SHALL BE ENCLOSED IN AN UPPER AND LOWER PLASTIC SHROUD

NDC00009-3124-03

CLINDAMYCIN INJECTION,USP

NSN, MFG P/N

6505012933319

NSN

6505-01-293-3319

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NDC00009-3124-03

CLINDAMYCIN INJECTION,USP

NSN, MFG P/N

6505012933319

NSN

6505-01-293-3319

MFG

PHARMACIA & UPJOHN COMPANY

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 150.000 MILLIGRAMS CLINDAMYCIN EQUIVALENT PER MILLILITER
ADMINISTRATION: INTRAVENOUS
FEATURES PROVIDED: STERILE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: CLINDAMYCIN INJECTION USP STERILE 150MG/ML 4ML VIAL 25S
PRIMARY CONTAINER CONTENT QUANTITY: 4.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL, SINGLE DOSE
SPECIAL FEATURES: 600 MG IN A SINGLE-DOSE,15 ML CAPACITY GLASS VIAL W/DOUBLED LEAD SCREW TO INTERLOCK W/INLET PORT OF DEXTROSE INJECTION,6505-01-260-1237,6505-01-260-1238,6505-01-260-1239 AND SODIUM CHLORIDE INJECTION,6505-01-260-1241,6505-01-260-1242,AND 6505-01-260-6715;
TOTAL PRIMARY CONTAINER QUANTITY: 25
~1: EACH DRUG VIAL SHALL BE ENCLOSED IN AN UPPER AND LOWER PLASTIC SHROUD

NDC51284-0468-02

TANNIC ACID GEL

NSN, MFG P/N

6505012935580

NSN

6505-01-293-5580

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NDC51284-0468-02

TANNIC ACID GEL

NSN, MFG P/N

6505012935580

NSN

6505-01-293-5580

MFG

ZILA PHARMACEUTICALS INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 7.000 PERCENTAGE, W/V TANNIC ACID ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: TANNIC ACID GEL 7% 0.25OZ TUBE
III SUPPLEMENTARY FEATURES: MEDSEP ITEM FOR DOD,ZILA PHARMACEUTICALS INC
PRIMARY CONTAINER CONTENT QUANTITY: 0.250 OUNCES
PRIMARY CONTAINER TYPE: TUBE
SPECIAL FEATURES: USE PREFERRED UPC: 3-50486-46802-4 IN ACCORDANCE WITH THE JDF