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Buspirone Hydrochloride - 63629-1747-2 - (Buspirone Hydrochloride)

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Drug Information of Buspirone Hydrochloride

Product NDC: 63629-1747
Proprietary Name: Buspirone Hydrochloride
Non Proprietary Name: Buspirone Hydrochloride
Active Ingredient(s): 15    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: 63629-1747
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075022
Marketing Category: ANDA
Start Marketing Date: 20020301

Package Information of Buspirone Hydrochloride

Package NDC: 63629-1747-2
Package Description: 100 TABLET in 1 BOTTLE (63629-1747-2)

NDC Information of Buspirone Hydrochloride

NDC Code 63629-1747-2
Proprietary Name Buspirone Hydrochloride
Package Description 100 TABLET in 1 BOTTLE (63629-1747-2)
Product NDC 63629-1747
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Buspirone Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20020301
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name BUSPIRONE HYDROCHLORIDE
Strength Number 15
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Buspirone Hydrochloride


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