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Chloroquine Phosphate
Chloroquine Phosphate - 0115-7010-01 - (CHLOROQUINE PHOSPHATE)
Drug Information of Chloroquine Phosphate
| Product NDC: | 0115-7010 |
| Proprietary Name: | Chloroquine Phosphate |
| Non Proprietary Name: | CHLOROQUINE PHOSPHATE |
| Active Ingredient(s): | 500 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: | 0115-7010 |
| Labeler Name: | Global Pharmaceuticals, Division of Impax Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040516 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20051101 |
Package Information of Chloroquine Phosphate
| Package NDC: | 0115-7010-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (0115-7010-01) |
NDC Information of Chloroquine Phosphate
| NDC Code | 0115-7010-01 |
| Proprietary Name | Chloroquine Phosphate |
| Package Description | 100 TABLET in 1 BOTTLE (0115-7010-01) |
| Product NDC | 0115-7010 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | CHLOROQUINE PHOSPHATE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20051101 |
| Marketing Category Name | ANDA |
| Labeler Name | Global Pharmaceuticals, Division of Impax Laboratories, Inc. |
| Substance Name | CHLOROQUINE PHOSPHATE |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antimalarial [EPC] |
