CIMETIDINE - 16590-372-30 - (CIMETIDINE)

Alphabetical Index


Drug Information of CIMETIDINE

Product NDC: 16590-372
Proprietary Name: CIMETIDINE
Non Proprietary Name: CIMETIDINE
Active Ingredient(s): 800    mg/1 & nbsp;   CIMETIDINE
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of CIMETIDINE

Product NDC: 16590-372
Labeler Name: STAT RX USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074424
Marketing Category: ANDA
Start Marketing Date: 20100526

Package Information of CIMETIDINE

Package NDC: 16590-372-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (16590-372-30)

NDC Information of CIMETIDINE

NDC Code 16590-372-30
Proprietary Name CIMETIDINE
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (16590-372-30)
Product NDC 16590-372
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CIMETIDINE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100526
Marketing Category Name ANDA
Labeler Name STAT RX USA LLC
Substance Name CIMETIDINE
Strength Number 800
Strength Unit mg/1
Pharmaceutical Classes Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

Complete Information of CIMETIDINE


General Information