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6505-01-009-1156

20 Products

NDC50962-0125-15

POTASSIUM CHLORIDE ORAL SOLUTION,USP

NSN, MFG P/N

6505010091156

NSN

6505-01-009-1156

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NDC50962-0125-15

POTASSIUM CHLORIDE ORAL SOLUTION,USP

NSN, MFG P/N

6505010091156

NSN

6505-01-009-1156

MFG

U S DEPT OF VETERANS AFFAIRS

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 1.333 MILLIEQUIVALENTS POTASSIUM CHLORIDE PER MILLILITER
FLAVOR: ANY ACCEPTABLE
PRIMARY CONTAINER CONTENT QUANTITY: 15.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: SUGAR FREE; CONTAINS ALCOHOL 5 PCT
TOTAL PRIMARY CONTAINER QUANTITY: 100

004-0065-23

FLURAZEPAM HYDROCHLORIDE CAPSULES,USP

NSN, MFG P/N

6505010091159

NSN

6505-01-009-1159

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004-0065-23

FLURAZEPAM HYDROCHLORIDE CAPSULES,USP

NSN, MFG P/N

6505010091159

NSN

6505-01-009-1159

MFG

HOFFMANN-LA ROCHE INC.

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 15.000 MILLIGRAMS FLURAZEPAM HYDROCHLORIDE ACTIVE INGREDIENT
CAPSULE CONTENT FORM: POWDER
CAPSULE PRIMARY CONTAINER CONTENT QUANTITY: 30.000
CAPSULE TYPE: HARD
PRIMARY CONTAINER TYPE: BOTTLE

DALMANE

FLURAZEPAM HYDROCHLORIDE CAPSULES,USP

NSN, MFG P/N

6505010091159

NSN

6505-01-009-1159

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DALMANE

FLURAZEPAM HYDROCHLORIDE CAPSULES,USP

NSN, MFG P/N

6505010091159

NSN

6505-01-009-1159

MFG

HOFFMANN-LA ROCHE INC.

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 15.000 MILLIGRAMS FLURAZEPAM HYDROCHLORIDE ACTIVE INGREDIENT
CAPSULE CONTENT FORM: POWDER
CAPSULE PRIMARY CONTAINER CONTENT QUANTITY: 30.000
CAPSULE TYPE: HARD
PRIMARY CONTAINER TYPE: BOTTLE

2897

MINERAL OIL LOTION,LANOLATED

NSN, MFG P/N

6505010092897

NSN

6505-01-009-2897

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2897

MINERAL OIL LOTION,LANOLATED

NSN, MFG P/N

6505010092897

NSN

6505-01-009-2897

MFG

ELITE MEDICAL PRODUCTS INC .

Description

III PART NAME ASSIGNED BY CONTROLLING AGENCY: MINERAL OIL LOTION LANOLATED 6.5 OZ BT
PRIMARY CONTAINER CONTENT QUANTITY: 6.500 OUNCES
PRIMARY CONTAINER TYPE: BOTTLE WITH FLIP-TOP CLOSURE
SPECIAL FEATURES: PH RANGE OF 5.0 TO 7.0;WHITE,SMOOTH LOTIO IN A BASE CONSISTING OF PURIFIED WATER,TRIETHANOLAMINE,DOCUSATE SODIUM,PROPYLENE GLYCOL,GLYCERYL STEARATE,PEG 40 STEARATE,PEG 4 DILAURATE,POLYOXYETHYLENE LAURYL ETHER,METHYLPARABEN,AND CARBOXYVINYL
~1: COPOLYMER;ADMINISTRATION:TOPICAL

NDC19810-0533-50

MINERAL OIL LOTION,LANOLATED

NSN, MFG P/N

6505010092897

NSN

6505-01-009-2897

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NDC19810-0533-50

MINERAL OIL LOTION,LANOLATED

NSN, MFG P/N

6505010092897

NSN

6505-01-009-2897

MFG

BRISTOL-MYERS SQUIBB CO P O BOX 5250 PRINCETON NJ 08543-5250

Description

III PART NAME ASSIGNED BY CONTROLLING AGENCY: MINERAL OIL LOTION LANOLATED 6.5 OZ BT
PRIMARY CONTAINER CONTENT QUANTITY: 6.500 OUNCES
PRIMARY CONTAINER TYPE: BOTTLE WITH FLIP-TOP CLOSURE
SPECIAL FEATURES: PH RANGE OF 5.0 TO 7.0;WHITE,SMOOTH LOTIO IN A BASE CONSISTING OF PURIFIED WATER,TRIETHANOLAMINE,DOCUSATE SODIUM,PROPYLENE GLYCOL,GLYCERYL STEARATE,PEG 40 STEARATE,PEG 4 DILAURATE,POLYOXYETHYLENE LAURYL ETHER,METHYLPARABEN,AND CARBOXYVINYL
~1: COPOLYMER;ADMINISTRATION:TOPICAL

NDC00409-3024-01

SODIUM NITROPRUSSIDE,USP

NSN, MFG P/N

6505010095019

NSN

6505-01-009-5019

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NDC00409-3024-01

SODIUM NITROPRUSSIDE,USP

NSN, MFG P/N

6505010095019

NSN

6505-01-009-5019

MFG

AMERISOURCEBERGEN DRUG CORPORATION DIV CORPORATE OFFICE

Description

III PART NAME ASSIGNED BY CONTROLLING AGENCY: SODIUM NITROPRUSSIDE STERILE USP 50MG
III SUPPLEMENTARY FEATURES: D-DAY ITEM FOR DOD
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 50.000 MILLIGRAMS
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: NOT FOR DIRECT INJECTION

NDC00003-0113-50

CEPHRADINE CAPSULES,USP

NSN, MFG P/N

6505010099531

NSN

6505-01-009-9531

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NDC00003-0113-50

CEPHRADINE CAPSULES,USP

NSN, MFG P/N

6505010099531

NSN

6505-01-009-9531

MFG

CARDINAL HEALTH 200 LLC

Description

(NON-CORE DATA) EXTERIOR CONTAINER QUANTITY: 144
(NON-CORE DATA) INTERMEDIATE PACKAGE QUANTITY: 12
(NON-CORE DATA) UNIT OF ISSUE CUBE: 0.029 CUBIC FEET
(NON-CORE DATA) UNIT OF ISSUE WEIGHT: 0.38 POUNDS
ACTIVE MEDICAMENT MEDICINAL STRENGTH: 250.000 MILLIGRAMS CEPHRADINE ACTIVE INGREDIENT
ADMINISTRATION: ORAL
CAPSULE CONTENT FORM: POWDER
CAPSULE PRIMARY CONTAINER CONTENT QUANTITY: 100.000
CAPSULE TYPE: ANY ACCEPTABLE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: CEPHRADINE CAPSULES USP 250MG 100S
PRIMARY CONTAINER TYPE: BOTTLE

ALUPENT

METAPROTERENOL SULFATE TABLETS,USP

NSN, MFG P/N

6505010103044

NSN

6505-01-010-3044

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ALUPENT

METAPROTERENOL SULFATE TABLETS,USP

NSN, MFG P/N

6505010103044

NSN

6505-01-010-3044

MFG

BOEHRINGER INGELHEIM PHARMACEUTICALS INC.

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 20.000 MILLIGRAMS METAPROTERENOL SULFATE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: METAPROTERENOL SULFATE TABLETS 20MG 100S BT
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

ALUPENT TABLETS

METAPROTERENOL SULFATE TABLETS,USP

NSN, MFG P/N

6505010103044

NSN

6505-01-010-3044

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ALUPENT TABLETS

METAPROTERENOL SULFATE TABLETS,USP

NSN, MFG P/N

6505010103044

NSN

6505-01-010-3044

MFG

BOEHRINGER INGELHEIM PHARMACEUTICALS INC.

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 20.000 MILLIGRAMS METAPROTERENOL SULFATE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: METAPROTERENOL SULFATE TABLETS 20MG 100S BT
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

NDC00043-0063-51

METAPROTERENOL SULFATE TABLETS,USP

NSN, MFG P/N

6505010103044

NSN

6505-01-010-3044

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NDC00043-0063-51

METAPROTERENOL SULFATE TABLETS,USP

NSN, MFG P/N

6505010103044

NSN

6505-01-010-3044

MFG

NOVARTIS PHARMACEUTICALS CORPORATION

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 20.000 MILLIGRAMS METAPROTERENOL SULFATE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: METAPROTERENOL SULFATE TABLETS 20MG 100S BT
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

NDC00182-1284-01

METAPROTERENOL SULFATE TABLETS,USP

NSN, MFG P/N

6505010103044

NSN

6505-01-010-3044

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NDC00182-1284-01

METAPROTERENOL SULFATE TABLETS,USP

NSN, MFG P/N

6505010103044

NSN

6505-01-010-3044

MFG

GOLDLINE LABORATORIES INC. DBA GOLDLINE LABORATORIES

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 20.000 MILLIGRAMS METAPROTERENOL SULFATE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: METAPROTERENOL SULFATE TABLETS 20MG 100S BT
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

NDC00332-2232-09

METAPROTERENOL SULFATE TABLETS,USP

NSN, MFG P/N

6505010103044

NSN

6505-01-010-3044

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NDC00332-2232-09

METAPROTERENOL SULFATE TABLETS,USP

NSN, MFG P/N

6505010103044

NSN

6505-01-010-3044

MFG

BIOCRAFT LABORATORIES INC CORPORATE HQ

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 20.000 MILLIGRAMS METAPROTERENOL SULFATE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: METAPROTERENOL SULFATE TABLETS 20MG 100S BT
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

NDC00597-0072-01

METAPROTERENOL SULFATE TABLETS,USP

NSN, MFG P/N

6505010103044

NSN

6505-01-010-3044

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NDC00597-0072-01

METAPROTERENOL SULFATE TABLETS,USP

NSN, MFG P/N

6505010103044

NSN

6505-01-010-3044

MFG

BOEHRINGER INGELHEIM PHARMACEUTICALS INC.

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 20.000 MILLIGRAMS METAPROTERENOL SULFATE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: METAPROTERENOL SULFATE TABLETS 20MG 100S BT
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

NDC49884-0259-01

METAPROTERENOL SULFATE TABLETS,USP

NSN, MFG P/N

6505010103044

NSN

6505-01-010-3044

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NDC49884-0259-01

METAPROTERENOL SULFATE TABLETS,USP

NSN, MFG P/N

6505010103044

NSN

6505-01-010-3044

MFG

PAR PHARMACEUTICAL INC.

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 20.000 MILLIGRAMS METAPROTERENOL SULFATE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: METAPROTERENOL SULFATE TABLETS 20MG 100S BT
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

NDC00052-0460-02

PYRIDOSTIGMINE BROMIDE INJECTION,USP

NSN, MFG P/N

6505010103050

NSN

6505-01-010-3050

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NDC00052-0460-02

PYRIDOSTIGMINE BROMIDE INJECTION,USP

NSN, MFG P/N

6505010103050

NSN

6505-01-010-3050

MFG

ORGANON USA INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 5.000 MILLIGRAMS PYRIDOSTIGMINE BROMIDE PER MILLILITER
PRIMARY CONTAINER CONTENT QUANTITY: 2.000 MILLILITERS
PRIMARY CONTAINER TYPE: AMPUL
TOTAL PRIMARY CONTAINER QUANTITY: 25

REGONOL INJECTION

PYRIDOSTIGMINE BROMIDE INJECTION,USP

NSN, MFG P/N

6505010103050

NSN

6505-01-010-3050

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REGONOL INJECTION

PYRIDOSTIGMINE BROMIDE INJECTION,USP

NSN, MFG P/N

6505010103050

NSN

6505-01-010-3050

MFG

ORGANON USA INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 5.000 MILLIGRAMS PYRIDOSTIGMINE BROMIDE PER MILLILITER
PRIMARY CONTAINER CONTENT QUANTITY: 2.000 MILLILITERS
PRIMARY CONTAINER TYPE: AMPUL
TOTAL PRIMARY CONTAINER QUANTITY: 25

019-5374-92

METHYCLOTHIAZIDE AN

NSN, MFG P/N

6505010103065

NSN

6505-01-010-3065

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019-5374-92

METHYCLOTHIAZIDE AN

NSN, MFG P/N

6505010103065

NSN

6505-01-010-3065

MFG

MALLINCKRODT INC ANESTHESIA PRODUCTS

Description

GENERAL CHARACTERISTICS ITEM DESCRIPTION: 2.5 MG METHYCLOTHIAZIDE,0.1 MG RESERPINE,SCORED,100 TABLETS PER BOTTLE

DIVTENSEN-R

METHYCLOTHIAZIDE AN

NSN, MFG P/N

6505010103065

NSN

6505-01-010-3065

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DIVTENSEN-R

METHYCLOTHIAZIDE AN

NSN, MFG P/N

6505010103065

NSN

6505-01-010-3065

MFG

MALLINCKRODT INC ANESTHESIA PRODUCTS

Description

GENERAL CHARACTERISTICS ITEM DESCRIPTION: 2.5 MG METHYCLOTHIAZIDE,0.1 MG RESERPINE,SCORED,100 TABLETS PER BOTTLE

781

TOBRAMYCIN INJECTION,USP

NSN, MFG P/N

6505010103066

NSN

6505-01-010-3066

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781

TOBRAMYCIN INJECTION,USP

NSN, MFG P/N

6505010103066

NSN

6505-01-010-3066

MFG

ELI LILLY AND COMPANY DBA ELI LILLY

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 40.000 MILLIGRAMS TOBRAMYCIN EQUIVALENT OF BASE PER MILLILITER
III PART NAME ASSIGNED BY CONTROLLING AGENCY: TOBRAMYCIN INJECTION USP 40MG/ML 2ML BT
III PROTECTIVE STORAGE FEATURE: SUBJECT TO DAMAGE BY FREEZING
PRIMARY CONTAINER CONTENT QUANTITY: 2.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL

NDC00002-1499-01

TOBRAMYCIN INJECTION,USP

NSN, MFG P/N

6505010103066

NSN

6505-01-010-3066

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NDC00002-1499-01

TOBRAMYCIN INJECTION,USP

NSN, MFG P/N

6505010103066

NSN

6505-01-010-3066

MFG

ELI LILLY AND COMPANY DBA ELI LILLY

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 40.000 MILLIGRAMS TOBRAMYCIN EQUIVALENT OF BASE PER MILLILITER
III PART NAME ASSIGNED BY CONTROLLING AGENCY: TOBRAMYCIN INJECTION USP 40MG/ML 2ML BT
III PROTECTIVE STORAGE FEATURE: SUBJECT TO DAMAGE BY FREEZING
PRIMARY CONTAINER CONTENT QUANTITY: 2.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL