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Chloroquine
Chloroquine - 0143-2125-01 - (Chloroquine Phosphate)
Drug Information of Chloroquine
| Product NDC: | 0143-2125 |
| 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: | 0143-2125 |
| Labeler Name: | West-ward Pharmaceutical Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA083082 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19990917 |
Package Information of Chloroquine
| Package NDC: | 0143-2125-01 |
| Package Description: | 100 TABLET, COATED in 1 BOTTLE, PLASTIC (0143-2125-01) |
NDC Information of Chloroquine
| NDC Code | 0143-2125-01 |
| Proprietary Name | Chloroquine |
| Package Description | 100 TABLET, COATED in 1 BOTTLE, PLASTIC (0143-2125-01) |
| Product NDC | 0143-2125 |
| 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 | West-ward Pharmaceutical Corp |
| Substance Name | CHLOROQUINE PHOSPHATE |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antimalarial [EPC] |
