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 | 71335-1771-8 | Bryant Ranch Prepack | ANDA040081 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 50090-5388-2 | A-S Medication Solutions | ANDA201691 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 42385-971-60 | Laurus Labs Limited | ANDA210959 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 59212-562-60 | Concordia Pharmaceuticals Inc. | NDA009768 | HUMAN PRESCRIPTION DRUG | NDA |
| HYDROXYCHLOROQUINE SULFATE | 71335-0897-4 | Bryant Ranch Prepack | ANDA040657 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 76420-643-01 | Asclemed USA, Inc. | ANDA210959 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 16729-485-16 | Accord Healthcare, Inc., | ANDA213342 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 76385-144-50 | Bayshore Pharmaceuticals LLC | ANDA040766 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 68382-096-77 | Zydus Pharmaceuticals USA Inc. | ANDA040657 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 43598-133-01 | Dr. Reddy's Laboratories Inc. | ANDA210441 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 70954-805-10 | ANI Pharmaceuticals, Inc. | NDA214581 | HUMAN PRESCRIPTION DRUG | NDA |
| HYDROXYCHLOROQUINE SULFATE | 16571-112-10 | Rising Pharma Holdings, Inc. | ANDA210959 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 57664-761-13 | Sun Pharmaceutical Industries, Inc. | ANDA201691 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 53002-4850-6 | RPK Pharmaceuticals, Inc. | ANDA040133 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 50090-4659-1 | A-S Medication Solutions | ANDA210577 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 0093-2401-01 | Teva Pharmaceuticals USA, Inc. | ANDA040081 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 76420-643-90 | Asclemed USA, Inc. | ANDA210959 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 16729-561-01 | Accord Healthcare, Inc., | ANDA213342 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 50090-5388-1 | A-S Medication Solutions | ANDA201691 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 70954-804-10 | ANI Pharmaceuticals, Inc. | NDA214581 | HUMAN PRESCRIPTION DRUG | NDA |
| HYDROXYCHLOROQUINE SULFATE | 43353-051-80 | Aphena Pharma Solutions - Tennessee, LLC | NDA009768 | HUMAN PRESCRIPTION DRUG | NDA AUTHORIZED GENERIC |
| HYDROXYCHLOROQUINE SULFATE | 71335-1771-7 | Bryant Ranch Prepack | ANDA040081 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 16571-687-01 | Rising Pharma Holdings, Inc. | ANDA210959 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 68071-2912-9 | NuCare Pharmaceuticals,Inc. | ANDA040657 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 42385-971-11 | Laurus Labs Limited | ANDA210959 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 68071-2912-3 | NuCare Pharmaceuticals,Inc. | ANDA040657 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 42385-971-05 | Laurus Labs Limited | ANDA210959 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 0904-7046-61 | Major Pharmaceuticals | ANDA210441 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 71335-1523-2 | Bryant Ranch Prepack | ANDA210577 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 76420-643-30 | Asclemed USA, Inc. | ANDA210959 | HUMAN PRESCRIPTION DRUG | ANDA |
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