Cimetidine - 0093-8204-05 - (Cimetidine)

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Drug Information of Cimetidine

Product NDC: 0093-8204
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: 0093-8204
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074151
Marketing Category: ANDA
Start Marketing Date: 20040202

Package Information of Cimetidine

Package NDC: 0093-8204-05
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE (0093-8204-05)

NDC Information of Cimetidine

NDC Code 0093-8204-05
Proprietary Name Cimetidine
Package Description 500 TABLET, FILM COATED in 1 BOTTLE (0093-8204-05)
Product NDC 0093-8204
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cimetidine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20040202
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA 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