BUSPIRONE HYDROCHLORIDE
- Product NDC
- 82804-039
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- BUSPIRONE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA078246
- Marketing category
- ANDA
- Substance
- BUSPIRONE HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 82804-039-20 | 20 TABLET in 1 BOTTLE (82804-039-20) | 2024-02-27 | | No | Historical |
| 82804-039-30 | 30 TABLET in 1 BOTTLE (82804-039-30) | 2023-11-07 | | No | Historical |
| 82804-039-60 | 60 TABLET in 1 BOTTLE (82804-039-60) | 2023-11-07 | | No | Historical |
| 82804-039-90 | 90 TABLET in 1 BOTTLE (82804-039-90) | 2023-11-07 | | No | Historical |