RANITIDINE - 64679-742-02 - (RANITIDINE HYDROCHLORIDE)

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Drug Information of RANITIDINE

Product NDC: 64679-742
Proprietary Name: RANITIDINE
Non Proprietary Name: RANITIDINE HYDROCHLORIDE
Active Ingredient(s): 300    mg/1 & nbsp;   RANITIDINE HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of RANITIDINE

Product NDC: 64679-742
Labeler Name: WOCKHARDT USA LLC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078701
Marketing Category: ANDA
Start Marketing Date: 20091211

Package Information of RANITIDINE

Package NDC: 64679-742-02
Package Description: 250 TABLET in 1 BOTTLE (64679-742-02)

NDC Information of RANITIDINE

NDC Code 64679-742-02
Proprietary Name RANITIDINE
Package Description 250 TABLET in 1 BOTTLE (64679-742-02)
Product NDC 64679-742
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name RANITIDINE HYDROCHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091211
Marketing Category Name ANDA
Labeler Name WOCKHARDT USA LLC.
Substance Name RANITIDINE HYDROCHLORIDE
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

Complete Information of RANITIDINE


General Information