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BUSPIRONE HYDROCHLORIDE - 24236-950-28 - (BUSPIRONE HYDROCHLORIDE)

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Drug Information of BUSPIRONE HYDROCHLORIDE

Product NDC: 24236-950
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: 24236-950
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075385
Marketing Category: ANDA
Start Marketing Date: 20101215

Package Information of BUSPIRONE HYDROCHLORIDE

Package NDC: 24236-950-28
Package Description: 300 TABLET in 1 CANISTER (24236-950-28)

NDC Information of BUSPIRONE HYDROCHLORIDE

NDC Code 24236-950-28
Proprietary Name BUSPIRONE HYDROCHLORIDE
Package Description 300 TABLET in 1 CANISTER (24236-950-28)
Product NDC 24236-950
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name BUSPIRONE HYDROCHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101215
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name BUSPIRONE HYDROCHLORIDE
Strength Number 15
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of BUSPIRONE HYDROCHLORIDE


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