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Buspirone HCl
Buspirone HCl - 21695-217-30 - (Buspirone hydrochloride)
Drug Information of Buspirone HCl
| Product NDC: | 21695-217 |
| Proprietary Name: | Buspirone HCl |
| 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 HCl
| Product NDC: | 21695-217 |
| Labeler Name: | Rebel Distributors Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074253 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20010328 |
Package Information of Buspirone HCl
| Package NDC: | 21695-217-30 |
| Package Description: | 30 TABLET in 1 BOTTLE (21695-217-30) |
NDC Information of Buspirone HCl
| NDC Code | 21695-217-30 |
| Proprietary Name | Buspirone HCl |
| Package Description | 30 TABLET in 1 BOTTLE (21695-217-30) |
| Product NDC | 21695-217 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Buspirone hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20010328 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp. |
| Substance Name | BUSPIRONE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
