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Buspirone Hydrochloride
Buspirone Hydrochloride - 52959-676-90 - (Buspirone Hydrochloride)
Drug Information of Buspirone Hydrochloride
| Product NDC: | 52959-676 |
| 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: | 52959-676 |
| Labeler Name: | H.J. Harkins Company, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075022 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101223 |
Package Information of Buspirone Hydrochloride
| Package NDC: | 52959-676-90 |
| Package Description: | 90 TABLET in 1 BOTTLE (52959-676-90) |
NDC Information of Buspirone Hydrochloride
| NDC Code | 52959-676-90 |
| Proprietary Name | Buspirone Hydrochloride |
| Package Description | 90 TABLET in 1 BOTTLE (52959-676-90) |
| Product NDC | 52959-676 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Buspirone Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20101223 |
| Marketing Category Name | ANDA |
| Labeler Name | H.J. Harkins Company, Inc. |
| Substance Name | BUSPIRONE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
