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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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 |
HYDROXYCHLOROQUINE SULFATE | 50090-2508-0 | A-S Medication Solutions | ANDA040133 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROXYCHLOROQUINE SULFATE | 82009-045-05 | Quallent Pharmaceuticals Health LLC | ANDA040657 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROXYCHLOROQUINE SULFATE | 0615-8459-39 | NCS HealthCare of KY, LLC dba Vangard Labs | ANDA040657 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROXYCHLOROQUINE SULFATE | 68084-269-01 | American Health Packaging | ANDA040657 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROXYCHLOROQUINE SULFATE | 50090-6629-0 | A-S Medication Solutions | ANDA040657 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROXYCHLOROQUINE SULFATE | 16729-563-16 | Accord Healthcare, Inc., | ANDA213342 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROXYCHLOROQUINE SULFATE | 43598-721-01 | Dr. Reddy's Laboratories Inc. | ANDA210441 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROXYCHLOROQUINE SULFATE | 76420-643-60 | Asclemed USA, Inc. | ANDA210959 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROXYCHLOROQUINE SULFATE | 71335-0897-8 | Bryant Ranch Prepack | ANDA040657 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROXYCHLOROQUINE SULFATE | 71610-701-80 | Aphena Pharma Solutions - Tennessee, LLC | ANDA210441 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROXYCHLOROQUINE SULFATE | 50090-5573-1 | A-S Medication Solutions | ANDA040657 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROXYCHLOROQUINE SULFATE | 16571-687-50 | 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 | 59212-562-10 | Concordia Pharmaceuticals Inc. | NDA009768 | HUMAN PRESCRIPTION DRUG | NDA |
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