Buspirone Hydrochloride
- Product NDC
- 71335-1924
- 11-digit product format
- 713351924
- Labeler code
- 71335
- Product ID
- 71335-1924_dc2d46ac-4db0-45ce-9001-19607d5f0906
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA210907
- Marketing category
- ANDA
- Marketing start
- 2019-11-14
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 5 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 207LT9J9OC | BUSPIRONE HYDROCHLORIDE | 33386-08-2 | BUSPIRONE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-1924-1 | 71335192401 | 90 TABLET in 1 BOTTLE, PLASTIC (71335-1924-1) | 90 tablet | 2021-08-12 | No | No | Historical |
| 71335-1924-2 | 71335192402 | 45 TABLET in 1 BOTTLE, PLASTIC (71335-1924-2) | 45 tablet | 2022-10-19 | No | No | Historical |
| 71335-1924-3 | 71335192403 | 30 TABLET in 1 BOTTLE, PLASTIC (71335-1924-3) | 30 tablet | 2021-12-13 | No | No | Historical |
| 71335-1924-4 | 71335192404 | 60 TABLET in 1 BOTTLE, PLASTIC (71335-1924-4) | 60 tablet | 2021-11-29 | No | No | Historical |
| 71335-1924-5 | 71335192405 | 180 TABLET in 1 BOTTLE, PLASTIC (71335-1924-5) | 180 tablet | 2024-04-05 | No | No | Historical |
| 71335-1924-6 | 71335192406 | 120 TABLET in 1 BOTTLE, PLASTIC (71335-1924-6) | 120 tablet | 2024-04-05 | No | No | Historical |