Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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 SODIUM 72888-111-05  Advagen Pharma Ltd  ANDA216548  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 72888-110-60  Advagen Pharma Ltd  ANDA216548  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 72888-110-05  Advagen Pharma Ltd  ANDA216548  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 72888-110-00  Advagen Pharma Ltd  ANDA216548  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 72888-109-00  Advagen Pharma Ltd  ANDA216548  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 72888-110-01  Advagen Pharma Ltd  ANDA216548  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 72888-109-01  Advagen Pharma Ltd  ANDA216548  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 72888-109-30  Advagen Pharma Ltd  ANDA216548  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 72888-111-00  Advagen Pharma Ltd  ANDA216548  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 72888-111-60  Advagen Pharma Ltd  ANDA216548  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 72888-109-05  Advagen Pharma Ltd  ANDA216548  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 72888-109-60  Advagen Pharma Ltd  ANDA216548  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 72888-111-01  Advagen Pharma Ltd  ANDA216548  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC SODIUM 72888-110-30  Advagen Pharma Ltd  ANDA216548  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC POTASSIUM 67877-772-58  Ascend Laboratories, LLC  ANDA216635  HUMAN PRESCRIPTION DRUG  ANDA 
DICLOFENAC POTASSIUM 67877-772-49  Ascend Laboratories, LLC  ANDA216635  HUMAN PRESCRIPTION DRUG  ANDA 
LIDOCAINE; DICLOFENAC SODIUM; MENTHOL, (+)- 73352-565-01  Trifluent Pharma LLC  M017  HUMAN OTC DRUG  OTC Monograph Drug 
DICLOFENAC SODIUM 0010-4498-01  Boehringer Ingelheim Animal Health USA Inc.  NADA141186  PRESCRIPTION ANIMAL DRUG  NADA 
DICLOFENAC SODIUM 0078-0478-61  Novartis Pharmaceutical Corporation  NDA020037  HUMAN PRESCRIPTION DRUG  NDA 
DICLOFENAC SODIUM 33358-451-30  RxChange Co.  NDA020254  HUMAN PRESCRIPTION DRUG  NDA AUTHORIZED GENERIC 
MISOPROSTOL; DICLOFENAC SODIUM 80425-0272-1  Advanced Rx Pharmacy of Tennessee, LLC  NDA020607  HUMAN PRESCRIPTION DRUG  NDA authorized generic 
DICLOFENAC SODIUM; MISOPROSTOL 59762-0028-2  Greenstone LLC  NDA020607  HUMAN PRESCRIPTION DRUG  NDA AUTHORIZED GENERIC 
DICLOFENAC SODIUM; MISOPROSTOL 59762-0029-1  Greenstone LLC  NDA020607  HUMAN PRESCRIPTION DRUG  NDA AUTHORIZED GENERIC 
MISOPROSTOL; DICLOFENAC SODIUM 0025-1411-90  Pfizer Laboratories Div Pfizer Inc  NDA020607  HUMAN PRESCRIPTION DRUG  NDA 
MISOPROSTOL; DICLOFENAC SODIUM 0025-1411-60  Pfizer Laboratories Div Pfizer Inc  NDA020607  HUMAN PRESCRIPTION DRUG  NDA 
DICLOFENAC SODIUM; MISOPROSTOL 59762-0028-1  Greenstone LLC  NDA020607  HUMAN PRESCRIPTION DRUG  NDA AUTHORIZED GENERIC 
DICLOFENAC SODIUM; MISOPROSTOL 21695-425-60  Rebel Distributors Corp.  NDA020607  HUMAN PRESCRIPTION DRUG  NDA 
DICLOFENAC SODIUM; MISOPROSTOL 0025-1421-60  Pfizer Laboratories Div Pfizer Inc  NDA020607  HUMAN PRESCRIPTION DRUG  NDA 
DICLOFENAC EPOLAMINE 83008-036-30  Quality Care Products, LLC  NDA021234  HUMAN PRESCRIPTION DRUG  NDA authorized generic 
DICLOFENAC EPOLAMINE 55700-886-30  Quality Care Products, LLC  NDA021234  HUMAN PRESCRIPTION DRUG  NDA authorized generic 
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
-
-