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U.S. Department of Health and Human Services

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 71610-047-60  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 
1-30 31-60 61-90 91-120 121-150 151-180 181-193

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