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Chloroquine - 55289-856-10 - (Chloroquine Phosphate)

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Drug Information of Chloroquine

Product NDC: 55289-856
Proprietary Name: Chloroquine
Non Proprietary Name: Chloroquine Phosphate
Active Ingredient(s): 500    mg/1 & nbsp;   Chloroquine Phosphate
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Chloroquine

Product NDC: 55289-856
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA083082
Marketing Category: ANDA
Start Marketing Date: 19990917

Package Information of Chloroquine

Package NDC: 55289-856-10
Package Description: 10 TABLET, COATED in 1 BOTTLE, PLASTIC (55289-856-10)

NDC Information of Chloroquine

NDC Code 55289-856-10
Proprietary Name Chloroquine
Package Description 10 TABLET, COATED in 1 BOTTLE, PLASTIC (55289-856-10)
Product NDC 55289-856
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Chloroquine Phosphate
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 19990917
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name CHLOROQUINE PHOSPHATE
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Antimalarial [EPC]

Complete Information of Chloroquine


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