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BUSPIRONE HYDROCHLORIDE - 16590-727-90 - (BUSPIRONE HYDROCHLORIDE)

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Drug Information of BUSPIRONE HYDROCHLORIDE

Product NDC: 16590-727
Proprietary Name: BUSPIRONE HYDROCHLORIDE
Non Proprietary Name: BUSPIRONE HYDROCHLORIDE
Active Ingredient(s): 7.5    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: 16590-727
Labeler Name: STAT RX USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075467
Marketing Category: ANDA
Start Marketing Date: 20100701

Package Information of BUSPIRONE HYDROCHLORIDE

Package NDC: 16590-727-90
Package Description: 90 TABLET in 1 BOTTLE (16590-727-90)

NDC Information of BUSPIRONE HYDROCHLORIDE

NDC Code 16590-727-90
Proprietary Name BUSPIRONE HYDROCHLORIDE
Package Description 90 TABLET in 1 BOTTLE (16590-727-90)
Product NDC 16590-727
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name BUSPIRONE HYDROCHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100701
Marketing Category Name ANDA
Labeler Name STAT RX USA LLC
Substance Name BUSPIRONE HYDROCHLORIDE
Strength Number 7.5
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of BUSPIRONE HYDROCHLORIDE


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