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Chloroquine
Chloroquine - 55289-856-40 - (Chloroquine Phosphate)
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: | 55289-856-40 |
| Package Description: | 40 TABLET, COATED in 1 BOTTLE, PLASTIC (55289-856-40) |
NDC Information of Chloroquine
| NDC Code | 55289-856-40 |
| Proprietary Name | Chloroquine |
| Package Description | 40 TABLET, COATED in 1 BOTTLE, PLASTIC (55289-856-40) |
| 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] |
