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Buspirone Hydrochloride - 49999-812-30 - (Buspirone Hydrochloride)

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Drug Information of Buspirone Hydrochloride

Product NDC: 49999-812
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: 49999-812
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074253
Marketing Category: ANDA
Start Marketing Date: 20101116

Package Information of Buspirone Hydrochloride

Package NDC: 49999-812-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (49999-812-30)

NDC Information of Buspirone Hydrochloride

NDC Code 49999-812-30
Proprietary Name Buspirone Hydrochloride
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (49999-812-30)
Product NDC 49999-812
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Buspirone Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101116
Marketing Category Name ANDA
Labeler Name Lake Erie Medical DBA Quality Care Products LLC
Substance Name BUSPIRONE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Buspirone Hydrochloride


General Information