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Ranitidine Hydrochloride - 49349-551-02 - (Ranitidine Hydrochloride)

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Drug Information of Ranitidine Hydrochloride

Product NDC: 49349-551
Proprietary Name: Ranitidine Hydrochloride
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 Hydrochloride

Product NDC: 49349-551
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077824
Marketing Category: ANDA
Start Marketing Date: 20111003

Package Information of Ranitidine Hydrochloride

Package NDC: 49349-551-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-551-02)

NDC Information of Ranitidine Hydrochloride

NDC Code 49349-551-02
Proprietary Name Ranitidine Hydrochloride
Package Description 30 TABLET in 1 BLISTER PACK (49349-551-02)
Product NDC 49349-551
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ranitidine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111003
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
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 Hydrochloride


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