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Chloroquine Phosphate - 0115-2790-06 - (CHLOROQUINE PHOSPHATE)

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Drug Information of Chloroquine Phosphate

Product NDC: 0115-2790
Proprietary Name: Chloroquine Phosphate
Non Proprietary Name: CHLOROQUINE PHOSPHATE
Active Ingredient(s): 250    mg/1 & nbsp;   CHLOROQUINE PHOSPHATE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Chloroquine Phosphate

Product NDC: 0115-2790
Labeler Name: Global Pharmaceuticals, Division of Impax Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA080880
Marketing Category: ANDA
Start Marketing Date: 19741211

Package Information of Chloroquine Phosphate

Package NDC: 0115-2790-06
Package Description: 50 TABLET in 1 BOTTLE (0115-2790-06)

NDC Information of Chloroquine Phosphate

NDC Code 0115-2790-06
Proprietary Name Chloroquine Phosphate
Package Description 50 TABLET in 1 BOTTLE (0115-2790-06)
Product NDC 0115-2790
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CHLOROQUINE PHOSPHATE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19741211
Marketing Category Name ANDA
Labeler Name Global Pharmaceuticals, Division of Impax Laboratories, Inc.
Substance Name CHLOROQUINE PHOSPHATE
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Antimalarial [EPC]

Complete Information of Chloroquine Phosphate


General Information