Buspirone Hydrochloride
- Product NDC
- 71335-9673
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- buspirone hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA075388
- Marketing category
- ANDA
- Substance
- BUSPIRONE HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 71335-9673-1 | 30 TABLET in 1 BOTTLE (71335-9673-1) | 2023-09-26 | | No | Historical |
| 71335-9673-2 | 60 TABLET in 1 BOTTLE (71335-9673-2) | 2023-07-13 | | No | Historical |
| 71335-9673-3 | 90 TABLET in 1 BOTTLE (71335-9673-3) | 2023-03-20 | | No | Historical |
| 71335-9673-4 | 45 TABLET in 1 BOTTLE (71335-9673-4) | 2024-04-03 | | No | Historical |
| 71335-9673-5 | 180 TABLET in 1 BOTTLE (71335-9673-5) | 2024-04-03 | | No | Historical |
| 71335-9673-6 | 120 TABLET in 1 BOTTLE (71335-9673-6) | 2024-04-03 | | No | Historical |
| 71335-9673-7 | 10 TABLET in 1 BOTTLE (71335-9673-7) | 2024-04-03 | | No | Historical |
| 71335-9673-8 | 100 TABLET in 1 BOTTLE (71335-9673-8) | 2024-04-03 | | No | Historical |