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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
CALCIPOTRIENE; NIACINAMIDE; DICLOFENAC SODIUM; HYALURONATE SODIUM 72934-2030-2  Sincerus Florida, LLC    HUMAN PRESCRIPTION DRUG  unapproved drug other 
DICLOFENAC SODIUM; CAPSAICIN 73247-201-01  Bodysphere, LLC  ANDA204132  HUMAN PRESCRIPTION DRUG  ANDA 
MENTHOL; DICLOFENAC SODIUM 73272-301-01  Upstream Pharma, LLC  ANDA203818  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC POTASSIUM 73352-086-30  Trifluent Pharma LLC  ANDA075229  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC POTASSIUM 73352-086-60  Trifluent Pharma LLC  ANDA075229  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC POTASSIUM 73352-095-60  Trifluent Pharma LLC  ANDA210078  HUMAN PRESCRIPTION DRUG  ANDA 
LIDOCAINE; MENTHOL, (+)-; DICLOFENAC SODIUM 73352-565-01  Trifluent Pharma LLC  M017  HUMAN OTC DRUG  OTC Monograph Drug 
DICLOFENAC SODIUM 73377-113-01  AX Pharmaceutical Corp    BULK INGREDIENT  bulk ingredient for animal drug compounding 
DICLOFENAC SODIUM 73469-2053-1  Scholl's Wellness Company  ANDA208077  HUMAN OTC DRUG  ANDA 
DICLOFENAC SODIUM 73469-2053-8  Scholl's Wellness Company  ANDA208077  HUMAN OTC DRUG  ANDA 
DICLOFENAC SODIUM 73516-450-01  Ashoka Health  ANDA204132  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM; CAPSAICIN 73516-801-01  Ashoka Health  ANDA204132  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 73581-104-15  YYBA CORP  ANDA210986  HUMAN OTC DRUG  ANDA 
DICLOFENAC POTASSIUM 73684-150-60  BLUCREST PHARMACEUTICALS, LLC  ANDA076561  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 73715-005-01  Mohnark Pharmaceuticals Inc.  ANDA210986  HUMAN OTC DRUG  ANDA 
DICLOFENAC POTASSIUM 74157-007-60  INA Pharmaceutics Inc  ANDA075229  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC POTASSIUM 74157-095-60  INA Pharmaceutics Inc.  ANDA210078  HUMAN PRESCRIPTION DRUG  ANDA 
MISOPROSTOL; DICLOFENAC SODIUM 75834-264-60  Nivagen Pharmaceuticals, Inc.  ANDA205143  HUMAN PRESCRIPTION DRUG  ANDA 
MISOPROSTOL; DICLOFENAC SODIUM 75834-264-90  Nivagen Pharmaceuticals, Inc.  ANDA205143  HUMAN PRESCRIPTION DRUG  ANDA 
MISOPROSTOL; DICLOFENAC SODIUM 75834-265-60  Nivagen Pharmaceuticals, Inc.  ANDA205143  HUMAN PRESCRIPTION DRUG  ANDA 
CAPSICUM OLEORESIN; OMEPRAZOLE; DICLOFENAC SODIUM 75840-094-01  GenPak Solutions, LLC  ANDA077863  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM; CAPSICUM OLEORESIN 75840-095-01  GenPak Solutions, LLC  ANDA077863  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 75987-040-05  Horizon Therapeutics USA, Inc.  NDA204623  HUMAN PRESCRIPTION DRUG  NDA 
DICLOFENAC SODIUM 75987-040-74  Horizon Therapeutics USA, Inc.  NDA204623  HUMAN PRESCRIPTION DRUG  NDA 
DICLOFENAC SODIUM 75987-040-75  Horizon Therapeutics USA, Inc.  NDA204623  HUMAN PRESCRIPTION DRUG  NDA 
DICLOFENAC SODIUM 76074-501-11  Two Hip Consulting, LLC    HUMAN PRESCRIPTION DRUG  unapproved drug other 
DICLOFENAC SODIUM 76282-663-39  EXELAN PHARMACEUTICALS INC.  ANDA209903  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 76420-012-30  Asclemed USA, Inc.  ANDA206116  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 76420-025-01  Asclemed USA, Inc.  ANDA200936  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 76420-091-01  Asclemed USA, Inc.  ANDA210986  HUMAN PRESCRIPTION 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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