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Buspirone Hydrochloride - 68788-9844-3 - (Buspirone Hydrochloride)

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Drug Information of Buspirone Hydrochloride

Product NDC: 68788-9844
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: 68788-9844
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075022
Marketing Category: ANDA
Start Marketing Date: 20120329

Package Information of Buspirone Hydrochloride

Package NDC: 68788-9844-3
Package Description: 30 TABLET in 1 BOTTLE (68788-9844-3)

NDC Information of Buspirone Hydrochloride

NDC Code 68788-9844-3
Proprietary Name Buspirone Hydrochloride
Package Description 30 TABLET in 1 BOTTLE (68788-9844-3)
Product NDC 68788-9844
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Buspirone Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120329
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc
Substance Name BUSPIRONE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Buspirone Hydrochloride


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