Product NDC: | 63629-1747 |
Proprietary Name: | Buspirone Hydrochloride |
Non Proprietary Name: | Buspirone Hydrochloride |
Active Ingredient(s): | 15 mg/1 & nbsp; Buspirone Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63629-1747 |
Labeler Name: | Bryant Ranch Prepack |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA075022 |
Marketing Category: | ANDA |
Start Marketing Date: | 20020301 |
Package NDC: | 63629-1747-2 |
Package Description: | 100 TABLET in 1 BOTTLE (63629-1747-2) |
NDC Code | 63629-1747-2 |
Proprietary Name | Buspirone Hydrochloride |
Package Description | 100 TABLET in 1 BOTTLE (63629-1747-2) |
Product NDC | 63629-1747 |
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 | Bryant Ranch Prepack |
Substance Name | BUSPIRONE HYDROCHLORIDE |
Strength Number | 15 |
Strength Unit | mg/1 |
Pharmaceutical Classes |