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Buspirone Hydrochloride
Buspirone Hydrochloride - 49884-725-05 - (buspirone hydrochloride)
Drug Information of Buspirone Hydrochloride
| Product NDC: | 49884-725 |
| 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: | 49884-725 |
| Labeler Name: | Par Pharmaceutical Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075467 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120423 |
Package Information of Buspirone Hydrochloride
| Package NDC: | 49884-725-05 |
| Package Description: | 500 TABLET in 1 BOTTLE (49884-725-05) |
NDC Information of Buspirone Hydrochloride
| NDC Code | 49884-725-05 |
| Proprietary Name | Buspirone Hydrochloride |
| Package Description | 500 TABLET in 1 BOTTLE (49884-725-05) |
| Product NDC | 49884-725 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | buspirone hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120423 |
| Marketing Category Name | ANDA |
| Labeler Name | Par Pharmaceutical Inc. |
| Substance Name | BUSPIRONE HYDROCHLORIDE |
| Strength Number | 7.5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
