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U.S. Department of Health and Human Services

FDA Application
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NDC Search Results on Active Ingredient: Diclofenac

Click on Active Ingredient to view the label.

Ingredient Name NDC Company Name Application Number or Regulatory Citation Product Type Marketing Category
DICLOFENAC SODIUM; MISOPROSTOL 68001-232-06  BluePoint Laboratories  ANDA201089  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 68001-279-00  BluePoint Laboratories  ANDA090066  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 68001-280-00  BluePoint Laboratories  ANDA090066  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 68001-280-06  BluePoint Laboratories  ANDA090066  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 68001-280-08  BluePoint Laboratories  ANDA090066  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 68001-281-00  BluePoint Laboratories  ANDA077863  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 68001-281-03  BluePoint Laboratories  ANDA077863  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 68001-281-06  BluePoint Laboratories  ANDA077863  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 68001-281-08  BluePoint Laboratories  ANDA077863  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 68001-612-00  BluePoint Laboratories  ANDA216275  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 68016-171-00  Chain Drug Consortium, LLC  ANDA208077  HUMAN OTC DRUG  ANDA 
DICLOFENAC SODIUM 68016-171-50  Chain Drug Consortium, LLC  ANDA208077  HUMAN OTC DRUG  ANDA 
DICLOFENAC SODIUM 68071-1653-5  NuCare Pharmaceuticals,Inc.  ANDA078031  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 68071-2045-3  NuCare Pharmaceuticals,Inc.  ANDA074514  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 68071-2045-6  NuCare Pharmaceuticals,Inc.  ANDA074514  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 68071-2045-9  NuCare Pharmaceuticals,Inc.  ANDA074514  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 68071-2223-7  NuCare Pharmaceuticals,Inc.  ANDA075492  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 68071-2239-1  NuCare Pharmaceuticals,Inc.  ANDA210986  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC POTASSIUM 68071-2625-3  NuCare Pharmaceuticals,Inc.  ANDA075229  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC POTASSIUM 68071-2625-9  NuCare Pharmaceuticals,Inc.  ANDA075229  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC POTASSIUM 68071-2892-3  NuCare Pharmaceuticals,Inc.  ANDA215585  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 68071-3184-1  NuCare Pharmaceuticals, Inc.  ANDA075185  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 68071-3184-2  NuCare Pharmaceuticals, Inc.  ANDA075185  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 68071-3184-3  NuCare Pharmaceuticals, Inc.  ANDA075185  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 68071-3184-5  NuCare Pharmaceuticals, Inc.  ANDA075185  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 68071-3184-6  NuCare Pharmaceuticals, Inc.  ANDA075185  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 68071-3184-9  NuCare Pharmaceuticals, Inc.  ANDA075185  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC POTASSIUM 68071-3451-3  NuCare Pharmaceuticals,Inc.  ANDA215750  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 68071-3456-1  NuCare Pharmaceuticals,Inc.  ANDA211253  HUMAN OTC DRUG  ANDA 
DICLOFENAC SODIUM 68071-3483-1  NuCare Pharmaceuticals,Inc.  ANDA210986  HUMAN OTC DRUG  ANDA 
1-30 31-60 61-90 91-120 121-150 151-180 181-210 211-240 241-270 271-300
301-330 331-360 361-390 391-420 421-450 451-480 481-510 511-540 541-570 571-600
601-630 631-660 661-690 691-720 721-750 751-780 781-810 811-840 841-870 871-900
901-930 931-960 961-990 991-1020 1021-1050 1051-1080 1081-1110 1111-1140 1141-1156

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