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Buspirone Hydrochloride - 54868-4568-1 - (Buspirone)

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Drug Information of Buspirone Hydrochloride

Product NDC: 54868-4568
Proprietary Name: Buspirone Hydrochloride
Non Proprietary Name: Buspirone
Active Ingredient(s): 10    mg/1 & nbsp;   Buspirone
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Buspirone Hydrochloride

Product NDC: 54868-4568
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074253
Marketing Category: ANDA
Start Marketing Date: 20090723

Package Information of Buspirone Hydrochloride

Package NDC: 54868-4568-1
Package Description: 30 TABLET in 1 BOTTLE (54868-4568-1)

NDC Information of Buspirone Hydrochloride

NDC Code 54868-4568-1
Proprietary Name Buspirone Hydrochloride
Package Description 30 TABLET in 1 BOTTLE (54868-4568-1)
Product NDC 54868-4568
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Buspirone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090723
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name BUSPIRONE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Buspirone Hydrochloride


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