Buspirone Hydrochloride
- Product NDC
- 71335-1930
- 11-digit product format
- 713351930
- Labeler code
- 71335
- Product ID
- 71335-1930_34f559ac-8751-5457-e063-6294a90af541
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA202330
- Marketing category
- ANDA
- Marketing start
- 2017-02-17
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 7.5 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 |
|---|
| 71335-1930-1 | 71335193001 | 30 TABLET in 1 BOTTLE (71335-1930-1) | 30 tablet | 2021-08-19 | No | No | Historical |
| 71335-1930-2 | 71335193002 | 90 TABLET in 1 BOTTLE (71335-1930-2) | 90 tablet | 2021-08-19 | No | No | Historical |
| 71335-1930-3 | 71335193003 | 18 TABLET in 1 BOTTLE (71335-1930-3) | 18 tablet | 2021-08-19 | No | No | Historical |
| 71335-1930-4 | 71335193004 | 28 TABLET in 1 BOTTLE (71335-1930-4) | 28 tablet | 2021-08-19 | No | No | Historical |
| 71335-1930-5 | 71335193005 | 60 TABLET in 1 BOTTLE (71335-1930-5) | 60 tablet | 2021-08-19 | No | No | Historical |