BUSPIRONE - 16590-600-90 - (BUSPIRONE HYDROCHLORIDE)

Alphabetical Index


Drug Information of BUSPIRONE

Product NDC: 16590-600
Proprietary Name: BUSPIRONE
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

Product NDC: 16590-600
Labeler Name: STAT RX USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075385
Marketing Category: ANDA
Start Marketing Date: 20020301

Package Information of BUSPIRONE

Package NDC: 16590-600-90
Package Description: 90 TABLET in 1 BOTTLE (16590-600-90)

NDC Information of BUSPIRONE

NDC Code 16590-600-90
Proprietary Name BUSPIRONE
Package Description 90 TABLET in 1 BOTTLE (16590-600-90)
Product NDC 16590-600
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name BUSPIRONE HYDROCHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20020301
Marketing Category Name ANDA
Labeler Name STAT RX USA LLC
Substance Name BUSPIRONE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of BUSPIRONE


General Information