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Buspirone Hydrochloride - 76237-122-30 - (Buspirone Hydrochloride)

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Drug Information of Buspirone Hydrochloride

Product NDC: 76237-122
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: 76237-122
Labeler Name: McKesson Contract Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075022
Marketing Category: ANDA
Start Marketing Date: 20111121

Package Information of Buspirone Hydrochloride

Package NDC: 76237-122-30
Package Description: 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-122-30) > 5 TABLET in 1 BLISTER PACK

NDC Information of Buspirone Hydrochloride

NDC Code 76237-122-30
Proprietary Name Buspirone Hydrochloride
Package Description 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-122-30) > 5 TABLET in 1 BLISTER PACK
Product NDC 76237-122
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Buspirone Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111121
Marketing Category Name ANDA
Labeler Name McKesson Contract Packaging
Substance Name BUSPIRONE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Buspirone Hydrochloride


General Information