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 | 16729-485-16 | Accord Healthcare, Inc., | ANDA213342 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 16729-563-16 | Accord Healthcare, Inc., | ANDA213342 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 16729-563-01 | Accord Healthcare, Inc., | ANDA213342 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 16729-485-01 | Accord Healthcare, Inc., | ANDA213342 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 16729-562-01 | Accord Healthcare, Inc., | ANDA213342 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 16729-561-01 | Accord Healthcare, Inc., | ANDA213342 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 68084-269-11 | American Health Packaging | ANDA040657 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 68084-269-01 | American Health Packaging | ANDA040657 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 60219-1544-1 | Amneal Pharmaceuticals NY LLC | ANDA210577 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 69238-1544-1 | Amneal Pharmaceuticals NY LLC | ANDA210577 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 69238-1544-5 | Amneal Pharmaceuticals NY LLC | ANDA210577 | HUMAN PRESCRIPTION DRUG | ANDA |
| CHLOROQUINE PHOSPHATE | 0115-2790-02 | Amneal Pharmaceuticals of New York LLC | ANDA080880 | HUMAN PRESCRIPTION DRUG | ANDA |
| CHLOROQUINE PHOSPHATE | 0115-7010-02 | Amneal Pharmaceuticals of New York LLC | ANDA040516 | HUMAN PRESCRIPTION DRUG | ANDA |
| CHLOROQUINE PHOSPHATE | 0115-7010-09 | Amneal Pharmaceuticals of New York LLC | ANDA040516 | HUMAN PRESCRIPTION DRUG | ANDA |
| CHLOROQUINE PHOSPHATE | 0115-2790-06 | Amneal Pharmaceuticals of New York LLC | ANDA080880 | HUMAN PRESCRIPTION DRUG | ANDA |
| CHLOROQUINE PHOSPHATE | 0115-7010-01 | Amneal Pharmaceuticals of New York LLC | ANDA040516 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 70954-805-10 | ANI Pharmaceuticals, Inc. | NDA214581 | HUMAN PRESCRIPTION DRUG | NDA |
| HYDROXYCHLOROQUINE SULFATE | 70954-804-10 | ANI Pharmaceuticals, Inc. | NDA214581 | HUMAN PRESCRIPTION DRUG | NDA |
| HYDROXYCHLOROQUINE SULFATE | 70954-804-30 | ANI Pharmaceuticals, Inc. | NDA214581 | HUMAN PRESCRIPTION DRUG | NDA |
| HYDROXYCHLOROQUINE SULFATE | 70954-805-20 | ANI Pharmaceuticals, Inc. | NDA214581 | HUMAN PRESCRIPTION DRUG | NDA |
| HYDROXYCHLOROQUINE SULFATE | 70954-804-20 | ANI Pharmaceuticals, Inc. | NDA214581 | HUMAN PRESCRIPTION DRUG | NDA |
| HYDROXYCHLOROQUINE SULFATE | 43353-051-60 | Aphena Pharma Solutions - Tennessee, LLC | NDA009768 | HUMAN PRESCRIPTION DRUG | NDA AUTHORIZED GENERIC |
| HYDROXYCHLOROQUINE SULFATE | 71610-506-30 | Aphena Pharma Solutions - Tennessee, LLC | ANDA040657 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 43353-051-09 | Aphena Pharma Solutions - Tennessee, LLC | NDA009768 | HUMAN PRESCRIPTION DRUG | NDA AUTHORIZED GENERIC |
| HYDROXYCHLOROQUINE SULFATE | 71610-473-53 | Aphena Pharma Solutions - Tennessee, LLC | NDA009768 | HUMAN PRESCRIPTION DRUG | NDA |
| HYDROXYCHLOROQUINE SULFATE | 71610-701-53 | Aphena Pharma Solutions - Tennessee, LLC | ANDA210441 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 71610-047-60 | Aphena Pharma Solutions - Tennessee, LLC | ANDA040104 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 71610-473-80 | Aphena Pharma Solutions - Tennessee, LLC | NDA009768 | HUMAN PRESCRIPTION DRUG | NDA |
| HYDROXYCHLOROQUINE SULFATE | 71610-473-04 | Aphena Pharma Solutions - Tennessee, LLC | NDA009768 | HUMAN PRESCRIPTION DRUG | NDA |
| HYDROXYCHLOROQUINE SULFATE | 71610-701-80 | Aphena Pharma Solutions - Tennessee, LLC | ANDA210441 | HUMAN PRESCRIPTION DRUG | ANDA |
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