• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

FDA Application

  • Print
  • Share
  • E-mail
-

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 POTASSIUM 12634-827-81  APOTHECA, INC  ANDA075229  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC POTASSIUM 12634-827-84  APOTHECA, INC  ANDA075229  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC POTASSIUM 12634-827-85  APOTHECA, INC  ANDA075229  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC POTASSIUM 12634-827-91  APOTHECA, INC  ANDA075229  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 13107-269-47  Aurolife Pharma LLC  ANDA213040  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC POTASSIUM 13913-008-11  Assertio Therapeutics, Inc.  NDA022202  HUMAN PRESCRIPTION DRUG  NDA 
DICLOFENAC POTASSIUM 13913-008-12  Assertio Therapeutics, Inc.  NDA022202  HUMAN PRESCRIPTION DRUG  NDA 
DICLOFENAC POTASSIUM 13913-008-94  Assertio Therapeutics, Inc.  NDA022202  HUMAN PRESCRIPTION DRUG  NDA 
DICLOFENAC POTASSIUM 13913-011-01  Assertio Therapeutics, Inc.  NDA022165  HUMAN PRESCRIPTION DRUG  NDA 
DICLOFENAC POTASSIUM 13913-011-19  Assertio Therapeutics, Inc.  NDA022165  HUMAN PRESCRIPTION DRUG  NDA 
DICLOFENAC POTASSIUM 13913-012-01  Assertio Therapeutics, Inc.  NDA022165  HUMAN PRESCRIPTION DRUG  NDA 
DICLOFENAC POTASSIUM 13913-012-02  Assertio Therapeutics, Inc.  NDA022165  HUMAN PRESCRIPTION DRUG  NDA 
DICLOFENAC POTASSIUM 13913-012-03  Assertio Therapeutics, Inc.  NDA022165  HUMAN PRESCRIPTION DRUG  NDA 
DICLOFENAC POTASSIUM 15370-180-10  CARWIN PHARMACEUTICAL ASSOCIATES, LLC  ANDA076561  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC POTASSIUM 15370-180-60  CARWIN PHARMACEUTICAL ASSOCIATES, LLC  ANDA076561  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC POTASSIUM 15370-185-30  CARWIN PHARMACEUTICAL ASSOCIATES, LLC  ANDA076561  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 16571-101-25  Rising Pharmaceuticals, Inc.  ANDA078553  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 16571-101-50  Rising Pharmaceuticals, Inc.  ANDA078553  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 16571-201-06  Rising Pharma Holdings, Inc.  ANDA077863  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 16571-201-10  Rising Pharma Holdings, Inc.  ANDA077863  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 16571-201-11  Rising Pharma Holdings, Inc.  ANDA077863  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 16571-201-50  Rising Pharma Holdings, Inc.  ANDA077863  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 16571-202-06  Rising Pharma Holdings, Inc.  ANDA090066  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 16571-202-10  Rising Pharma Holdings, Inc.  ANDA090066  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 16571-202-11  Rising Pharma Holdings, Inc.  ANDA090066  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 16571-203-10  Rising Pharma Holdings, Inc.  ANDA090066  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 17856-0833-1  ATLANTIC BIOLOGICALS CORP.  ANDA208077  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 21130-028-10  Safeway, Inc.  ANDA208077  HUMAN OTC DRUG  ANDA 
DICLOFENAC SODIUM 21130-028-50  Safeway, Inc.  ANDA208077  HUMAN OTC DRUG  ANDA 
DICLOFENAC SODIUM 21130-313-01  Safeway  ANDA211253  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

Return to the FDA Label Search Page

-
-