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 |
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CHLOROQUINE PHOSPHATE | 37662-0273-2 | Hahnemann Laboratories, INC. | HUMAN OTC DRUG | unapproved homeopathic | |
CHLOROQUINE PHOSPHATE | 37662-0271-1 | Hahnemann Laboratories, INC. | HUMAN OTC DRUG | unapproved homeopathic | |
CHLOROQUINE PHOSPHATE | 37662-0266-1 | Hahnemann Laboratories, INC. | HUMAN OTC DRUG | unapproved homeopathic | |
CHLOROQUINE PHOSPHATE | 37662-0271-2 | Hahnemann Laboratories, INC. | HUMAN OTC DRUG | unapproved homeopathic | |
CHLOROQUINE PHOSPHATE | 37662-0271-4 | Hahnemann Laboratories, INC. | HUMAN OTC DRUG | unapproved homeopathic | |
HYDROXYCHLOROQUINE SULFATE | 60219-1544-1 | Amneal Pharmaceuticals NY LLC | ANDA210577 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROXYCHLOROQUINE SULFATE | 68084-269-11 | American Health Packaging | ANDA040657 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROXYCHLOROQUINE SULFATE | 0904-7046-06 | Major Pharmaceuticals | ANDA210441 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROXYCHLOROQUINE SULFATE | 16571-112-10 | Rising Pharma Holdings, Inc. | ANDA210959 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROXYCHLOROQUINE SULFATE | 71335-1771-5 | Bryant Ranch Prepack | ANDA040081 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROXYCHLOROQUINE SULFATE | 16729-563-01 | Accord Healthcare, Inc., | ANDA213342 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROXYCHLOROQUINE SULFATE | 68071-2912-2 | NuCare Pharmaceuticals,Inc. | ANDA040657 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROXYCHLOROQUINE SULFATE | 68788-7747-3 | Preferred Pharmaceuticals, Inc. | ANDA040657 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROXYCHLOROQUINE SULFATE | 42385-971-01 | Laurus Labs Limited | ANDA210959 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROXYCHLOROQUINE SULFATE | 50268-412-11 | AvPAK | ANDA210441 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROXYCHLOROQUINE SULFATE | 50090-3432-1 | A-S Medication Solutions | NDA009768 | HUMAN PRESCRIPTION DRUG | NDA AUTHORIZED GENERIC |
HYDROXYCHLOROQUINE SULFATE | 65841-633-05 | Zydus Lifesciences Limited | ANDA040657 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROXYCHLOROQUINE SULFATE | 50090-5573-2 | A-S Medication Solutions | ANDA040657 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROXYCHLOROQUINE SULFATE | 71205-448-12 | Proficient Rx LP | NDA009768 | HUMAN PRESCRIPTION DRUG | NDA |
HYDROXYCHLOROQUINE SULFATE | 55154-3567-0 | Cardinal Health 107, LLC | ANDA210441 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROXYCHLOROQUINE SULFATE | 68382-096-01 | Zydus Pharmaceuticals USA Inc. | ANDA040657 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROXYCHLOROQUINE SULFATE | 16714-110-02 | Northstar Rx LLC. | ANDA040657 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLOROQUINE PHOSPHATE | 0115-7010-09 | Amneal Pharmaceuticals of New York LLC | ANDA040516 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROXYCHLOROQUINE SULFATE | 16729-485-01 | Accord Healthcare, Inc., | ANDA213342 | HUMAN PRESCRIPTION DRUG | ANDA |
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 |
CHLOROQUINE PHOSPHATE | 64980-178-10 | Rising Pharmaceuticals, Inc. | ANDA090612 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROXYCHLOROQUINE SULFATE | 50090-2508-2 | A-S Medication Solutions | ANDA040133 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLOROQUINE PHOSPHATE | 64980-177-01 | Rising Pharmaceuticals, Inc. | ANDA091621 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROXYCHLOROQUINE SULFATE | 71335-0897-9 | Bryant Ranch Prepack | ANDA040657 | HUMAN PRESCRIPTION DRUG | ANDA |
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