• 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 Application Number: 075805

Click on Proprietary Name to view the label.

Proprietary Name NDC Company Name Application Number or Regulatory Citation Product Type Marketing Category
Famotidine 49999-237-30  Quality Care Products LLC  ANDA075805  HUMAN PRESCRIPTION DRUG  ANDA 
Famotidine 49999-230-60  Quality Care Products LLC  ANDA075805  HUMAN PRESCRIPTION DRUG  ANDA 
Famotidine 67296-0963-1  RedPharm Drug, Inc.  ANDA075805  HUMAN PRESCRIPTION DRUG  ANDA 
Famotidine 70518-1001-1  REMEDYREPACK INC.  ANDA075805  HUMAN PRESCRIPTION DRUG  ANDA 
Famotidine 70518-0461-1  REMEDYREPACK INC.  ANDA075805  HUMAN PRESCRIPTION DRUG  ANDA 
Famotidine 70518-1001-0  REMEDYREPACK INC.  ANDA075805  HUMAN PRESCRIPTION DRUG  ANDA 
Famotidine 70518-0461-0  REMEDYREPACK INC.  ANDA075805  HUMAN PRESCRIPTION DRUG  ANDA 
Famotidine 53002-3199-0  RPK Pharmaceuticals, Inc.  ANDA075805  HUMAN PRESCRIPTION DRUG  ANDA 
Famotidine 53002-3199-3  RPK Pharmaceuticals, Inc.  ANDA075805  HUMAN PRESCRIPTION DRUG  ANDA 
Famotidine 53002-6672-2  RPK Pharmaceuticals, Inc.  ANDA075805  HUMAN PRESCRIPTION DRUG  ANDA 
Famotidine 53002-6672-3  RPK Pharmaceuticals, Inc.  ANDA075805  HUMAN PRESCRIPTION DRUG  ANDA 
Famotidine 53002-3199-2  RPK Pharmaceuticals, Inc.  ANDA075805  HUMAN PRESCRIPTION DRUG  ANDA 
Famotidine 53002-3199-5  RPK Pharmaceuticals, Inc.  ANDA075805  HUMAN PRESCRIPTION DRUG  ANDA 
Famotidine 53002-3199-6  RPK Pharmaceuticals, Inc.  ANDA075805  HUMAN PRESCRIPTION DRUG  ANDA 
Famotidine 53002-6672-1  RPK Pharmaceuticals, Inc.  ANDA075805  HUMAN PRESCRIPTION DRUG  ANDA 
Famotidine 53002-6672-6  RPK Pharmaceuticals, Inc.  ANDA075805  HUMAN PRESCRIPTION DRUG  ANDA 
Famotidine 60760-327-07  St. Mary's Medical Park Pharmacy  ANDA075805  HUMAN PRESCRIPTION DRUG  ANDA 
Famotidine 60760-327-60  St. Mary's Medical Park Pharmacy  ANDA075805  HUMAN PRESCRIPTION DRUG  ANDA 
Famotidine 50436-7371-3  Unit Dose Services  ANDA075805  HUMAN PRESCRIPTION DRUG  ANDA 
Famotidine 50436-7371-2  Unit Dose Services  ANDA075805  HUMAN PRESCRIPTION DRUG  ANDA 
Famotidine 50436-7371-1  Unit Dose Services  ANDA075805  HUMAN PRESCRIPTION DRUG  ANDA 
1-30 31-60 61-90 91-120 121-141

Return to the FDA Label Search Page

-
-