FDA Application
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NDC Search Results on Active Ingredient: Chloroquine
Click on Active Ingredient to view the label.
| Ingredient Name | NDC | Company Name | Application Number or Regulatory Citation | Product Type | Marketing Category |
|---|---|---|---|---|---|
| HYDROXYCHLOROQUINE SULFATE | 50090-4659-3 | A-S Medication Solutions | ANDA210577 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 71335-1771-3 | Bryant Ranch Prepack | ANDA040081 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 42385-927-05 | Laurus Labs Limited | ANDA210959 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 68382-096-05 | Zydus Pharmaceuticals USA Inc. | ANDA040657 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 43353-051-53 | Aphena Pharma Solutions - Tennessee, LLC | NDA009768 | HUMAN PRESCRIPTION DRUG | NDA AUTHORIZED GENERIC |
| HYDROXYCHLOROQUINE SULFATE | 71335-1771-2 | Bryant Ranch Prepack | ANDA040081 | HUMAN PRESCRIPTION DRUG | ANDA |
| CHLOROQUINE PHOSPHATE | 0115-7010-01 | Amneal Pharmaceuticals of New York LLC | ANDA040516 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 71335-1523-5 | Bryant Ranch Prepack | ANDA210577 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 53808-1112-1 | DOH CENTRAL PHARMACY | ANDA040766 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 71610-473-30 | Aphena Pharma Solutions - Tennessee, LLC | NDA009768 | HUMAN PRESCRIPTION DRUG | NDA |
| CHLOROQUINE PHOSPHATE | 64980-178-05 | Rising Pharmaceuticals, Inc. | ANDA090612 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 55154-2074-0 | Cardinal Health 107, LLC | ANDA040657 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 67296-1780-1 | RedPharm Drug, Inc. | ANDA040104 | HUMAN PRESCRIPTION DRUG | ANDA |
| 1-30 | 31-60 | 61-90 | 91-120 | 121-150 | 151-180 | 181-193 |
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