CIMETIDINE - 49349-096-02 - (CIMETIDINE)

Alphabetical Index


Drug Information of CIMETIDINE

Product NDC: 49349-096
Proprietary Name: CIMETIDINE
Non Proprietary Name: CIMETIDINE
Active Ingredient(s): 400    mg/1 & nbsp;   CIMETIDINE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of CIMETIDINE

Product NDC: 49349-096
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074890
Marketing Category: ANDA
Start Marketing Date: 20101124

Package Information of CIMETIDINE

Package NDC: 49349-096-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-096-02)

NDC Information of CIMETIDINE

NDC Code 49349-096-02
Proprietary Name CIMETIDINE
Package Description 30 TABLET in 1 BLISTER PACK (49349-096-02)
Product NDC 49349-096
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CIMETIDINE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101124
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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