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Buspirone Hydrochloride - 52125-260-02 - (Buspirone Hydrochloride)

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Drug Information of Buspirone Hydrochloride

Product NDC: 52125-260
Proprietary Name: Buspirone Hydrochloride
Non Proprietary Name: Buspirone Hydrochloride
Active Ingredient(s): 5    mg/1 & nbsp;   Buspirone Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Buspirone Hydrochloride

Product NDC: 52125-260
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075022
Marketing Category: ANDA
Start Marketing Date: 20130503

Package Information of Buspirone Hydrochloride

Package NDC: 52125-260-02
Package Description: 30 TABLET in 1 BLISTER PACK (52125-260-02)

NDC Information of Buspirone Hydrochloride

NDC Code 52125-260-02
Proprietary Name Buspirone Hydrochloride
Package Description 30 TABLET in 1 BLISTER PACK (52125-260-02)
Product NDC 52125-260
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Buspirone Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130503
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name BUSPIRONE HYDROCHLORIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Buspirone Hydrochloride


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