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 | 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 | 71205-448-12 | Proficient Rx LP | NDA009768 | HUMAN PRESCRIPTION DRUG | NDA |
| HYDROXYCHLOROQUINE SULFATE | 16571-112-01 | Rising Pharma Holdings, Inc. | ANDA210959 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 16571-112-06 | Rising Pharma Holdings, Inc. | ANDA210959 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 50090-2508-2 | A-S Medication Solutions | ANDA040133 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 70954-804-30 | ANI Pharmaceuticals, Inc. | NDA214581 | HUMAN PRESCRIPTION DRUG | NDA |
| HYDROXYCHLOROQUINE SULFATE | 43353-051-09 | Aphena Pharma Solutions - Tennessee, LLC | NDA009768 | HUMAN PRESCRIPTION DRUG | NDA AUTHORIZED GENERIC |
| HYDROXYCHLOROQUINE SULFATE | 59212-562-11 | Concordia Pharmaceuticals Inc. | NDA009768 | HUMAN PRESCRIPTION DRUG | NDA |
| HYDROXYCHLOROQUINE SULFATE | 71335-1771-9 | Bryant Ranch Prepack | ANDA040081 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 42385-927-01 | Laurus Labs Limited | ANDA210959 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 50090-6280-2 | A-S Medication Solutions | ANDA213342 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 50268-412-15 | AvPAK | ANDA210441 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 71335-1523-3 | Bryant Ranch Prepack | ANDA210577 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 71610-047-60 | Aphena Pharma Solutions - Tennessee, LLC | ANDA040104 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 71335-0897-9 | Bryant Ranch Prepack | ANDA040657 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 71610-473-80 | Aphena Pharma Solutions - Tennessee, LLC | NDA009768 | HUMAN PRESCRIPTION DRUG | NDA |
| HYDROXYCHLOROQUINE SULFATE | 43598-132-05 | Dr. Reddy's Laboratories Inc. | ANDA210441 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 43598-131-05 | Dr. Reddy's Laboratories Inc. | ANDA210441 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 71335-1523-9 | Bryant Ranch Prepack | ANDA210577 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 68071-2332-1 | NuCare Pharmaceuticals,Inc. | ANDA040657 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 71335-0897-5 | Bryant Ranch Prepack | ANDA040657 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 71610-473-04 | Aphena Pharma Solutions - Tennessee, LLC | NDA009768 | HUMAN PRESCRIPTION DRUG | NDA |
| HYDROXYCHLOROQUINE SULFATE | 16714-110-01 | Northstar Rx LLC. | ANDA040657 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 57664-761-88 | Sun Pharmaceutical Industries, Inc. | ANDA201691 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 71335-1771-1 | Bryant Ranch Prepack | ANDA040081 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 50090-2508-1 | A-S Medication Solutions | ANDA040133 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 50090-4659-2 | A-S Medication Solutions | ANDA210577 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 71335-0897-1 | Bryant Ranch Prepack | ANDA040657 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 50090-3432-2 | A-S Medication Solutions | NDA009768 | HUMAN PRESCRIPTION DRUG | NDA AUTHORIZED GENERIC |
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