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 | 0093-2401-01 | Teva Pharmaceuticals USA, Inc. | ANDA040081 | HUMAN PRESCRIPTION DRUG | ANDA |
| CHLOROQUINE PHOSPHATE | 0115-2790-02 | Amneal Pharmaceuticals of New York LLC | ANDA080880 | 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 |
| 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 |
| HYDROXYCHLOROQUINE SULFATE | 0615-8459-39 | NCS HealthCare of KY, LLC dba Vangard Labs | ANDA040657 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 0904-7046-06 | Major Pharmaceuticals | ANDA210441 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 0904-7046-61 | Major Pharmaceuticals | ANDA210441 | HUMAN PRESCRIPTION DRUG | ANDA |
| 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 | 16571-112-10 | Rising Pharma Holdings, Inc. | ANDA210959 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 16571-112-50 | Rising Pharma Holdings, Inc. | ANDA210959 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 16571-687-01 | Rising Pharma Holdings, Inc. | ANDA210959 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 16571-687-50 | Rising Pharma Holdings, Inc. | ANDA210959 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 16714-110-01 | Northstar Rx LLC. | ANDA040657 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 16714-110-02 | Northstar Rx LLC. | ANDA040657 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 16729-485-01 | Accord Healthcare, Inc., | ANDA213342 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 16729-485-16 | Accord Healthcare, Inc., | ANDA213342 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 16729-561-01 | Accord Healthcare, Inc., | ANDA213342 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 16729-562-01 | Accord Healthcare, Inc., | ANDA213342 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 16729-563-01 | Accord Healthcare, Inc., | ANDA213342 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROXYCHLOROQUINE SULFATE | 16729-563-16 | Accord Healthcare, Inc., | ANDA213342 | HUMAN PRESCRIPTION DRUG | ANDA |
| CHLOROQUINE PHOSPHATE | 23155-850-74 | Avet Pharmaceuticals Inc. | ANDA214756 | HUMAN PRESCRIPTION DRUG | ANDA |
| CHLOROQUINE PHOSPHATE | 37662-0266-1 | Hahnemann Laboratories, INC. | HUMAN OTC DRUG | unapproved homeopathic | |
| CHLOROQUINE PHOSPHATE | 37662-0266-2 | Hahnemann Laboratories, INC. | HUMAN OTC DRUG | unapproved homeopathic | |
| CHLOROQUINE PHOSPHATE | 37662-0266-3 | Hahnemann Laboratories, INC. | HUMAN OTC DRUG | unapproved homeopathic | |
| CHLOROQUINE PHOSPHATE | 37662-0267-1 | Hahnemann Laboratories, INC. | HUMAN OTC DRUG | unapproved homeopathic | |
| CHLOROQUINE PHOSPHATE | 37662-0267-2 | Hahnemann Laboratories, INC. | HUMAN OTC DRUG | unapproved homeopathic | |
| CHLOROQUINE PHOSPHATE | 37662-0267-3 | Hahnemann Laboratories, INC. | HUMAN OTC DRUG | unapproved homeopathic |
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