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Buspirone Hydrochloride - 0093-5200-05 - (Buspirone Hydrochloride)

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Drug Information of Buspirone Hydrochloride

Product NDC: 0093-5200
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: 0093-5200
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075022
Marketing Category: ANDA
Start Marketing Date: 20040326

Package Information of Buspirone Hydrochloride

Package NDC: 0093-5200-05
Package Description: 500 TABLET in 1 BOTTLE (0093-5200-05)

NDC Information of Buspirone Hydrochloride

NDC Code 0093-5200-05
Proprietary Name Buspirone Hydrochloride
Package Description 500 TABLET in 1 BOTTLE (0093-5200-05)
Product NDC 0093-5200
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Buspirone Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20040326
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name BUSPIRONE HYDROCHLORIDE
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Buspirone Hydrochloride


General Information