Buspirone Hydrochloride
- Product NDC
- 50090-5886
- 11-digit product format
- 500905886
- Labeler code
- 50090
- Product ID
- 50090-5886_1667fb24-4776-43db-b29b-3cfa228d82d0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA075022
- Marketing category
- ANDA
- Marketing start
- 2002-03-01
- 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 |
|---|
| 50090-5886-0 | 50090588600 | 500 TABLET in 1 BOTTLE (50090-5886-0) | 500 tablet | 2021-12-28 | No | No | Historical |
| 50090-5886-1 | 50090588601 | 60 TABLET in 1 BOTTLE (50090-5886-1) | 60 tablet | 2021-12-28 | No | No | Historical |
| 50090-5886-3 | 50090588603 | 90 TABLET in 1 BOTTLE (50090-5886-3) | 90 tablet | 2021-12-28 | No | No | Historical |