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Buspirone Hydrochloride - 55111-472-60 - (Buspirone Hydrochloride)

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Drug Information of Buspirone Hydrochloride

Product NDC: 55111-472
Proprietary Name: Buspirone Hydrochloride
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 Hydrochloride

Product NDC: 55111-472
Labeler Name: Dr. Reddy's Laboratories Ltd
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078246
Marketing Category: ANDA
Start Marketing Date: 20090304

Package Information of Buspirone Hydrochloride

Package NDC: 55111-472-60
Package Description: 60 TABLET in 1 BOTTLE (55111-472-60)

NDC Information of Buspirone Hydrochloride

NDC Code 55111-472-60
Proprietary Name Buspirone Hydrochloride
Package Description 60 TABLET in 1 BOTTLE (55111-472-60)
Product NDC 55111-472
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Buspirone Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090304
Marketing Category Name ANDA
Labeler Name Dr. Reddy's Laboratories Ltd
Substance Name BUSPIRONE HYDROCHLORIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Buspirone Hydrochloride


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