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6505-00-770-2061

20 Products

NDC43567-0540-01

AMITRIPTYLINE HYDROCHLORIDE TABLETS,USP

NSN, MFG P/N

6505007702061

NSN

6505-00-770-2061

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NDC43567-0540-01

AMITRIPTYLINE HYDROCHLORIDE TABLETS,USP

NSN, MFG P/N

6505007702061

NSN

6505-00-770-2061

MFG

MD PHARMACEUTICAL CO

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 50.000 MILLIGRAMS AMITRIPTYLINE HYDROCHLORIDE ACTIVE INGREDIENT
ADMINISTRATION: ORAL
III PART NAME ASSIGNED BY CONTROLLING AGENCY: AMITRIPTYLINE HYDROCHLORIDE TABLETS USP 50MG 100S BT
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE
THERAPEUTIC EQUIVALENT: ENDEP BY ROCHE

NDC00310-0041-10

AMITRIPTYLINE HYDROCHLORIDE TABLETS,USP

NSN, MFG P/N

6505007702061

NSN

6505-00-770-2061

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NDC00310-0041-10

AMITRIPTYLINE HYDROCHLORIDE TABLETS,USP

NSN, MFG P/N

6505007702061

NSN

6505-00-770-2061

MFG

ASTRAZENECA LP

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 50.000 MILLIGRAMS AMITRIPTYLINE HYDROCHLORIDE ACTIVE INGREDIENT
ADMINISTRATION: ORAL
III PART NAME ASSIGNED BY CONTROLLING AGENCY: AMITRIPTYLINE HYDROCHLORIDE TABLETS USP 50MG 100S BT
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE
THERAPEUTIC EQUIVALENT: ENDEP BY ROCHE

NDC00364-0575-01

AMITRIPTYLINE HYDROCHLORIDE TABLETS,USP

NSN, MFG P/N

6505007702061

NSN

6505-00-770-2061

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NDC00364-0575-01

AMITRIPTYLINE HYDROCHLORIDE TABLETS,USP

NSN, MFG P/N

6505007702061

NSN

6505-00-770-2061

MFG

SCHEIN PHARMACEUTICAL INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 50.000 MILLIGRAMS AMITRIPTYLINE HYDROCHLORIDE ACTIVE INGREDIENT
ADMINISTRATION: ORAL
III PART NAME ASSIGNED BY CONTROLLING AGENCY: AMITRIPTYLINE HYDROCHLORIDE TABLETS USP 50MG 100S BT
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE
THERAPEUTIC EQUIVALENT: ENDEP BY ROCHE

NDC00603-2214-21

AMITRIPTYLINE HYDROCHLORIDE TABLETS,USP

NSN, MFG P/N

6505007702061

NSN

6505-00-770-2061

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NDC00603-2214-21

AMITRIPTYLINE HYDROCHLORIDE TABLETS,USP

NSN, MFG P/N

6505007702061

NSN

6505-00-770-2061

MFG

GENERICS BIDCO I LLC DBA QUALITEST PHARMACEUTICALS

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 50.000 MILLIGRAMS AMITRIPTYLINE HYDROCHLORIDE ACTIVE INGREDIENT
ADMINISTRATION: ORAL
III PART NAME ASSIGNED BY CONTROLLING AGENCY: AMITRIPTYLINE HYDROCHLORIDE TABLETS USP 50MG 100S BT
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE
THERAPEUTIC EQUIVALENT: ENDEP BY ROCHE

NDC00781-1488-01

AMITRIPTYLINE HYDROCHLORIDE TABLETS,USP

NSN, MFG P/N

6505007702061

NSN

6505-00-770-2061

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NDC00781-1488-01

AMITRIPTYLINE HYDROCHLORIDE TABLETS,USP

NSN, MFG P/N

6505007702061

NSN

6505-00-770-2061

MFG

SANDOZ INC.

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 50.000 MILLIGRAMS AMITRIPTYLINE HYDROCHLORIDE ACTIVE INGREDIENT
ADMINISTRATION: ORAL
III PART NAME ASSIGNED BY CONTROLLING AGENCY: AMITRIPTYLINE HYDROCHLORIDE TABLETS USP 50MG 100S BT
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE
THERAPEUTIC EQUIVALENT: ENDEP BY ROCHE

18A

DEXTROSE AND SODIUM CHLORIDE INJECTION,USP

NSN, MFG P/N

6505007707344

NSN

6505-00-770-7344

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18A

DEXTROSE AND SODIUM CHLORIDE INJECTION,USP

NSN, MFG P/N

6505007707344

NSN

6505-00-770-7344

MFG

B BRAUN MEDICAL INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 5.000 PERCENTAGE, W/W DEXTROSE ACTIVE INGREDIENT AND 0.200 PERCENTAGE, W/W SODIUM CHLORIDE ACTIVE INGREDIENT
PHARMACEUTICAL VEHICLE TYPE: ANY ACCEPTABLE
PRIMARY CONTAINER CONTENT QUANTITY: 500.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE

413-27

DEXTROSE AND SODIUM CHLORIDE INJECTION,USP

NSN, MFG P/N

6505007707344

NSN

6505-00-770-7344

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413-27

DEXTROSE AND SODIUM CHLORIDE INJECTION,USP

NSN, MFG P/N

6505007707344

NSN

6505-00-770-7344

MFG

CUTTER LABORATORIES INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 5.000 PERCENTAGE, W/W DEXTROSE ACTIVE INGREDIENT AND 0.200 PERCENTAGE, W/W SODIUM CHLORIDE ACTIVE INGREDIENT
PHARMACEUTICAL VEHICLE TYPE: ANY ACCEPTABLE
PRIMARY CONTAINER CONTENT QUANTITY: 500.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE

NDC00003-0122-50

AMPICILLIN CAPSULES,USP

NSN, MFG P/N

6505007708343

NSN

6505-00-770-8343

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NDC00003-0122-50

AMPICILLIN CAPSULES,USP

NSN, MFG P/N

6505007708343

NSN

6505-00-770-8343

MFG

BRISTOL-MYERS CO

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 250.000 MILLIGRAMS AMPICILLIN EQUIVALENT
CAPSULE CONTENT FORM: ANY ACCEPTABLE
CAPSULE PRIMARY CONTAINER CONTENT QUANTITY: 100.000
CAPSULE TYPE: ANY ACCEPTABLE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: AMPICILLIN CAPSULES USP 250 MG 100S
PRIMARY CONTAINER TYPE: BOTTLE
PROTECTIVE STORAGE FEATURE: EXPIRATION DATED

NDC00093-5145-01

AMPICILLIN CAPSULES,USP

NSN, MFG P/N

6505007708343

NSN

6505-00-770-8343

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NDC00093-5145-01

AMPICILLIN CAPSULES,USP

NSN, MFG P/N

6505007708343

NSN

6505-00-770-8343

MFG

LEMMON CO

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 250.000 MILLIGRAMS AMPICILLIN EQUIVALENT
CAPSULE CONTENT FORM: ANY ACCEPTABLE
CAPSULE PRIMARY CONTAINER CONTENT QUANTITY: 100.000
CAPSULE TYPE: ANY ACCEPTABLE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: AMPICILLIN CAPSULES USP 250 MG 100S
PRIMARY CONTAINER TYPE: BOTTLE
PROTECTIVE STORAGE FEATURE: EXPIRATION DATED

POLYCILLIN

AMPICILLIN CAPSULES,USP

NSN, MFG P/N

6505007708343

NSN

6505-00-770-8343

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POLYCILLIN

AMPICILLIN CAPSULES,USP

NSN, MFG P/N

6505007708343

NSN

6505-00-770-8343

MFG

MEAD JOHNSON & COMPANY DBA MEAD JOHNSON NUTRITIONALS

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 250.000 MILLIGRAMS AMPICILLIN EQUIVALENT
CAPSULE CONTENT FORM: ANY ACCEPTABLE
CAPSULE PRIMARY CONTAINER CONTENT QUANTITY: 100.000
CAPSULE TYPE: ANY ACCEPTABLE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: AMPICILLIN CAPSULES USP 250 MG 100S
PRIMARY CONTAINER TYPE: BOTTLE
PROTECTIVE STORAGE FEATURE: EXPIRATION DATED

NDC00024-1322-08

NALIDIXIC ACID TABLETS,USP

NSN, MFG P/N

6505007708345

NSN

6505-00-770-8345

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NDC00024-1322-08

NALIDIXIC ACID TABLETS,USP

NSN, MFG P/N

6505007708345

NSN

6505-00-770-8345

MFG

STERLING-WINTHROP RESEARCH INSTITUTE A DIV OF STERLING DRUG INC

Description

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

NEGGRAM

NALIDIXIC ACID TABLETS,USP

NSN, MFG P/N

6505007708345

NSN

6505-00-770-8345

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NEGGRAM

NALIDIXIC ACID TABLETS,USP

NSN, MFG P/N

6505007708345

NSN

6505-00-770-8345

MFG

STERLING-WINTHROP RESEARCH INSTITUTE A DIV OF STERLING DRUG INC

Description

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

NEGGRAM TABLETS

NALIDIXIC ACID TABLETS,USP

NSN, MFG P/N

6505007708345

NSN

6505-00-770-8345

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NEGGRAM TABLETS

NALIDIXIC ACID TABLETS,USP

NSN, MFG P/N

6505007708345

NSN

6505-00-770-8345

MFG

STERLING-WINTHROP RESEARCH INSTITUTE A DIV OF STERLING DRUG INC

Description

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

DIAL0SE

DIOCTYL SODIUM SULFOSUCCINATE AND CARBOXYMETHYLCELLULOSE SODIUM CAPSULES

NSN, MFG P/N

6505007715272

NSN

6505-00-771-5272

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DIAL0SE

DIOCTYL SODIUM SULFOSUCCINATE AND CARBOXYMETHYLCELLULOSE SODIUM CAPSULES

NSN, MFG P/N

6505007715272

NSN

6505-00-771-5272

MFG

ZENECA INC ZENECA PHARMACEUTICALS GROUP STUART PHARMACEUTICALS

Description

CAPSULE CONTENT FORM: POWDER
CAPSULE PRIMARY CONTAINER CONTENT QUANTITY: 100.000
CAPSULE TYPE: HARD
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: ACTIVE MEDICAMENT MEDICINAL STRENGTH:400.000 MILLIGRAMS OF CARBOXYMETHYLCELLULOSE SODIUM ACTIVE INGREDIENTS;100.000 MILLIGRAMS OF DIOCTYL SODIUM SULFOSUCCINATE ACTIVE INGREDIENTS

MYLANTA

ALUMINUM HYDROXIDE GEL,MAGNESIUM HYDROXIDE,AND SIMETHICONE SUSPENSION

NSN, MFG P/N

6505007719207

NSN

6505-00-771-9207

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MYLANTA

ALUMINUM HYDROXIDE GEL,MAGNESIUM HYDROXIDE,AND SIMETHICONE SUSPENSION

NSN, MFG P/N

6505007719207

NSN

6505-00-771-9207

MFG

ZENECA INC ZENECA PHARMACEUTICALS GROUP STUART PHARMACEUTICALS

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: EACH 5 ML CONTAINS 40 MG ALUMINUMHYDROXIDE,40 MG MAGNESIUM HYDROXIDE,AND 20 MG SIMETHICONE
FLAVOR: ANY ACCEPTABLE
PHARMACEUTICAL VEHICLE TYPE: ANY ACCEPTABLE
PRIMARY CONTAINER CONTENT QUANTITY: 12.000 FLUID OUNCES OR 360.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE

NDC00038-0610-12

ALUMINUM HYDROXIDE GEL,MAGNESIUM HYDROXIDE,AND SIMETHICONE SUSPENSION

NSN, MFG P/N

6505007719207

NSN

6505-00-771-9207

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NDC00038-0610-12

ALUMINUM HYDROXIDE GEL,MAGNESIUM HYDROXIDE,AND SIMETHICONE SUSPENSION

NSN, MFG P/N

6505007719207

NSN

6505-00-771-9207

MFG

ZENECA INC ZENECA PHARMACEUTICALS GROUP STUART PHARMACEUTICALS

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: EACH 5 ML CONTAINS 40 MG ALUMINUMHYDROXIDE,40 MG MAGNESIUM HYDROXIDE,AND 20 MG SIMETHICONE
FLAVOR: ANY ACCEPTABLE
PHARMACEUTICAL VEHICLE TYPE: ANY ACCEPTABLE
PRIMARY CONTAINER CONTENT QUANTITY: 12.000 FLUID OUNCES OR 360.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE

NDC00182-1007-39

ALUMINUM HYDROXIDE GEL,MAGNESIUM HYDROXIDE,AND SIMETHICONE SUSPENSION

NSN, MFG P/N

6505007719207

NSN

6505-00-771-9207

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NDC00182-1007-39

ALUMINUM HYDROXIDE GEL,MAGNESIUM HYDROXIDE,AND SIMETHICONE SUSPENSION

NSN, MFG P/N

6505007719207

NSN

6505-00-771-9207

MFG

GOLDLINE LABORATORIES INC. DBA GOLDLINE LABORATORIES

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: EACH 5 ML CONTAINS 40 MG ALUMINUMHYDROXIDE,40 MG MAGNESIUM HYDROXIDE,AND 20 MG SIMETHICONE
FLAVOR: ANY ACCEPTABLE
PHARMACEUTICAL VEHICLE TYPE: ANY ACCEPTABLE
PRIMARY CONTAINER CONTENT QUANTITY: 12.000 FLUID OUNCES OR 360.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE

201-50

LIDOCAINE HYDROCHLORIDE INJECTION,USP

NSN, MFG P/N

6505007719234

NSN

6505-00-771-9234

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201-50

LIDOCAINE HYDROCHLORIDE INJECTION,USP

NSN, MFG P/N

6505007719234

NSN

6505-00-771-9234

MFG

LYPHOMED INC DIV OF FUJISAWA USA INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 1.000 PERCENTAGE, W/V LIDOCAINE HYDROCHLORIDE ACTIVE INGREDIENT
III PROTECTIVE STORAGE FEATURE: SUBJECT TO DAMAGE BY FREEZING
PRIMARY CONTAINER CONTENT QUANTITY: 50.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL
SPECIAL FEATURES: WITHOUT EPINEPHRINE; MULTIPLE DOSE VIAL

452390

LIDOCAINE HYDROCHLORIDE INJECTION,USP

NSN, MFG P/N

6505007719234

NSN

6505-00-771-9234

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452390

LIDOCAINE HYDROCHLORIDE INJECTION,USP

NSN, MFG P/N

6505007719234

NSN

6505-00-771-9234

MFG

ELKINS-SINN INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 1.000 PERCENTAGE, W/V LIDOCAINE HYDROCHLORIDE ACTIVE INGREDIENT
III PROTECTIVE STORAGE FEATURE: SUBJECT TO DAMAGE BY FREEZING
PRIMARY CONTAINER CONTENT QUANTITY: 50.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL
SPECIAL FEATURES: WITHOUT EPINEPHRINE; MULTIPLE DOSE VIAL

NDC00185-0221-26

LIDOCAINE HYDROCHLORIDE INJECTION,USP

NSN, MFG P/N

6505007719234

NSN

6505-00-771-9234

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NDC00185-0221-26

LIDOCAINE HYDROCHLORIDE INJECTION,USP

NSN, MFG P/N

6505007719234

NSN

6505-00-771-9234

MFG

VITARINE CO INC THE

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 1.000 PERCENTAGE, W/V LIDOCAINE HYDROCHLORIDE ACTIVE INGREDIENT
III PROTECTIVE STORAGE FEATURE: SUBJECT TO DAMAGE BY FREEZING
PRIMARY CONTAINER CONTENT QUANTITY: 50.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL
SPECIAL FEATURES: WITHOUT EPINEPHRINE; MULTIPLE DOSE VIAL