Cimetidine - 0093-8305-01 - (Cimetidine)

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Drug Information of Cimetidine

Product NDC: 0093-8305
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: 0093-8305
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074463
Marketing Category: ANDA
Start Marketing Date: 20031206

Package Information of Cimetidine

Package NDC: 0093-8305-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (0093-8305-01)

NDC Information of Cimetidine

NDC Code 0093-8305-01
Proprietary Name Cimetidine
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (0093-8305-01)
Product NDC 0093-8305
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cimetidine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20031206
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
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