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: Simvastatin

Click on Active Ingredient to view the label.

Ingredient Name NDC Company Name Application Number or Regulatory Citation Product Type Marketing Category
SIMVASTATIN; EZETIMIBE 43598-743-90  Dr.Reddys Laboratories Inc  ANDA200909  HUMAN PRESCRIPTION DRUG  ANDA 
SIMVASTATIN; EZETIMIBE 68462-323-90  Glenmark Pharmaceuticals Inc., USA  ANDA208699  HUMAN PRESCRIPTION DRUG  ANDA 
SIMVASTATIN; EZETIMIBE 60429-880-10  Golden State Medical Supply, Inc.  ANDA200909  HUMAN PRESCRIPTION DRUG  ANDA 
SIMVASTATIN; EZETIMIBE 21695-339-30  Rebel Distributors Corp.  NDA021687  HUMAN PRESCRIPTION DRUG  NDA 
SIMVASTATIN; EZETIMIBE 42291-078-10  AvKARE  ANDA208831  HUMAN PRESCRIPTION DRUG  ANDA 
SIMVASTATIN; EZETIMIBE 69238-1158-3  Amneal Pharmaceuticals NY LLC  ANDA208831  HUMAN PRESCRIPTION DRUG  ANDA 
SIMVASTATIN; EZETIMIBE 78206-175-01  Organon LLC  NDA021687  HUMAN PRESCRIPTION DRUG  NDA 
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
901-930 931-937

Return to the FDA Label Search Page
-
-