Buspirone Hydrochloride
- Product NDC
- 72162-1927
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- buspirone hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA078302
- Marketing category
- ANDA
- Substance
- BUSPIRONE HYDROCHLORIDE
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 72162-1927-5 | 500 TABLET in 1 BOTTLE (72162-1927-5) | 2020-05-01 | No | Historical | |
| 72162-1927-6 | 60 TABLET in 1 BOTTLE (72162-1927-6) | 2020-05-01 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| Buspirone Hydrochloride - Bryant Ranch Prepack | Bryant Ranch Prepack | 2025-11-04 | HUMAN PRESCRIPTION DRUG LABEL | 102 |
| Buspirone Hydrochloride - Bryant Ranch Prepack | Bryant Ranch Prepack | 2024-04-03 | HUMAN PRESCRIPTION DRUG LABEL | 101 |