Buspirone Hydrochloride
- Product NDC
- 72162-1926
- 11-digit product format
- 721621926
- Labeler code
- 72162
- Product ID
- 72162-1926_b3436f64-108a-4fc2-941e-39364842589c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- buspirone hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA075388
- Marketing category
- ANDA
- Marketing start
- 2020-07-27
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 15 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 |
|---|
| 72162-1926-1 | 72162192601 | 100 TABLET in 1 BOTTLE (72162-1926-1) | 100 tablet | 2020-07-27 | No | No | Historical |
| 72162-1926-5 | 72162192605 | 500 TABLET in 1 BOTTLE (72162-1926-5) | 500 tablet | 2020-07-27 | No | No | Historical |