Buspirone Hydrochloride
- Product NDC
- 50090-7742
- 11-digit product format
- 500907742
- Labeler code
- 50090
- Product ID
- 50090-7742_61f62c95-086e-451e-a2c1-9e286a4a0e88
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- buspirone hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA078302
- Marketing category
- ANDA
- Marketing start
- 2020-05-01
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 30 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 |
|---|
| 50090-7742-0 | 50090774200 | 60 TABLET in 1 BOTTLE (50090-7742-0) | 60 tablet | 2025-10-29 | No | No | Historical |
| 50090-7742-1 | 50090774201 | 90 TABLET in 1 BOTTLE (50090-7742-1) | 90 tablet | 2025-10-29 | No | No | Historical |