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 |
|---|---|---|---|---|---|
| CHLOROQUINE PHOSPHATE | 76385-142-05 | Bayshore Pharmaceuticals LLC | ANDA090610 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 43598-132-05 | Dr. Reddy's Laboratories Inc. | ANDA210441 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 50090-3432-2 | A-S Medication Solutions | NDA009768 | HUMAN PRESCRIPTION DRUG | NDA AUTHORIZED GENERIC |
| HYDROXYCHLOROQUINE SULFATE | 68071-2332-1 | NuCare Pharmaceuticals,Inc. | ANDA040657 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 50090-6629-0 | A-S Medication Solutions | ANDA040657 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 71610-473-80 | Aphena Pharma Solutions - Tennessee, LLC | NDA009768 | HUMAN PRESCRIPTION DRUG | NDA |
| HYDROXYCHLOROQUINE SULFATE | 59212-562-11 | Concordia Pharmaceuticals Inc. | NDA009768 | HUMAN PRESCRIPTION DRUG | NDA |
| CHLOROQUINE PHOSPHATE | 64980-177-10 | Rising Pharmaceuticals, Inc. | ANDA091621 | HUMAN PRESCRIPTION DRUG | ANDA |
| CHLOROQUINE PHOSPHATE | 0115-7010-02 | Amneal Pharmaceuticals of New York LLC | ANDA040516 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 71335-0897-6 | Bryant Ranch Prepack | ANDA040657 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 68071-4648-1 | NuCare Pharmaceuticals,Inc. | ANDA040657 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 71335-1523-7 | Bryant Ranch Prepack | ANDA210577 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 0904-7046-61 | Major Pharmaceuticals | ANDA210441 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 43598-132-01 | Dr. Reddy's Laboratories Inc. | ANDA210441 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 71335-1523-2 | Bryant Ranch Prepack | ANDA210577 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 42385-971-05 | Laurus Labs Limited | ANDA210959 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 71335-0897-7 | Bryant Ranch Prepack | ANDA040657 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 43353-051-60 | Aphena Pharma Solutions - Tennessee, LLC | NDA009768 | HUMAN PRESCRIPTION DRUG | NDA AUTHORIZED GENERIC |
| CHLOROQUINE PHOSPHATE | 68022-0264-1 | Suven Pharmaceuticals Limited | ANDA214756 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 71335-1771-6 | Bryant Ranch Prepack | ANDA040081 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 71335-0897-3 | Bryant Ranch Prepack | ANDA040657 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 76420-643-30 | Asclemed USA, Inc. | ANDA210959 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 76385-144-01 | Bayshore Pharmaceuticals LLC | ANDA040766 | 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 |
| HYDROXYCHLOROQUINE SULFATE | 65841-633-30 | Zydus Lifesciences Limited | ANDA040657 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 68788-7747-2 | Preferred Pharmaceuticals, Inc. | ANDA040657 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 67296-1781-1 | RedPharm Drug, Inc. | NDA009768 | HUMAN PRESCRIPTION DRUG | NDA |
| CHLOROQUINE PHOSPHATE | 64980-178-02 | Rising Pharmaceuticals, Inc. | ANDA090612 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 50090-6280-1 | A-S Medication Solutions | ANDA213342 | HUMAN PRESCRIPTION DRUG | ANDA |
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