Cimetidine - 54868-3315-2 - (Cimetidine)

Alphabetical Index


Drug Information of Cimetidine

Product NDC: 54868-3315
Proprietary Name: Cimetidine
Non Proprietary Name: Cimetidine
Active Ingredient(s): 400    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: 54868-3315
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074424
Marketing Category: ANDA
Start Marketing Date: 19940725

Package Information of Cimetidine

Package NDC: 54868-3315-2
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-3315-2)

NDC Information of Cimetidine

NDC Code 54868-3315-2
Proprietary Name Cimetidine
Package Description 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-3315-2)
Product NDC 54868-3315
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cimetidine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19940725
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name CIMETIDINE
Strength Number 400
Strength Unit mg/1
Pharmaceutical Classes Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

Complete Information of Cimetidine


General Information