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Buspirone HCl - 21695-256-60 - (Buspirone hydrochloride)

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Drug Information of Buspirone HCl

Product NDC: 21695-256
Proprietary Name: Buspirone HCl
Non Proprietary Name: Buspirone hydrochloride
Active Ingredient(s): 5    mg/1 & nbsp;   Buspirone hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Buspirone HCl

Product NDC: 21695-256
Labeler Name: Rebel Distributors Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074253
Marketing Category: ANDA
Start Marketing Date: 20010328

Package Information of Buspirone HCl

Package NDC: 21695-256-60
Package Description: 60 TABLET in 1 BOTTLE (21695-256-60)

NDC Information of Buspirone HCl

NDC Code 21695-256-60
Proprietary Name Buspirone HCl
Package Description 60 TABLET in 1 BOTTLE (21695-256-60)
Product NDC 21695-256
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Buspirone hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20010328
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp.
Substance Name BUSPIRONE HYDROCHLORIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Buspirone HCl


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