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Buspirone Hydrochloride - 0378-1175-91 - (buspirone hydrochloride)

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Drug Information of Buspirone Hydrochloride

Product NDC: 0378-1175
Proprietary Name: Buspirone Hydrochloride
Non Proprietary Name: buspirone hydrochloride
Active Ingredient(s): 30    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: 0378-1175
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076008
Marketing Category: ANDA
Start Marketing Date: 20111005

Package Information of Buspirone Hydrochloride

Package NDC: 0378-1175-91
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC (0378-1175-91)

NDC Information of Buspirone Hydrochloride

NDC Code 0378-1175-91
Proprietary Name Buspirone Hydrochloride
Package Description 60 TABLET in 1 BOTTLE, PLASTIC (0378-1175-91)
Product NDC 0378-1175
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name buspirone hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111005
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals Inc.
Substance Name BUSPIRONE HYDROCHLORIDE
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Buspirone Hydrochloride


General Information