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Buspirone Hydrochloride - 52959-676-90 - (Buspirone Hydrochloride)

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Drug Information of Buspirone Hydrochloride

Product NDC: 52959-676
Proprietary Name: Buspirone Hydrochloride
Non Proprietary Name: Buspirone Hydrochloride
Active Ingredient(s): 10    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: 52959-676
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075022
Marketing Category: ANDA
Start Marketing Date: 20101223

Package Information of Buspirone Hydrochloride

Package NDC: 52959-676-90
Package Description: 90 TABLET in 1 BOTTLE (52959-676-90)

NDC Information of Buspirone Hydrochloride

NDC Code 52959-676-90
Proprietary Name Buspirone Hydrochloride
Package Description 90 TABLET in 1 BOTTLE (52959-676-90)
Product NDC 52959-676
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Buspirone Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101223
Marketing Category Name ANDA
Labeler Name H.J. Harkins Company, Inc.
Substance Name BUSPIRONE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Buspirone Hydrochloride


General Information