BUSPIRONE HYDROCHLORIDE
- Product NDC
- 50090-7075
- 11-digit product format
- 500907075
- Labeler code
- 50090
- Product ID
- 50090-7075_ddd3d399-ddda-4d53-8fc5-a27e71b21b49
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- BUSPIRONE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA078246
- Marketing category
- ANDA
- Marketing start
- 2020-02-21
- 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 |
|---|
| 50090-7075-0 | 50090707500 | 60 TABLET in 1 BOTTLE (50090-7075-0) | 60 tablet | 2024-01-25 | No | No | Historical |
| 50090-7075-1 | 50090707501 | 90 TABLET in 1 BOTTLE (50090-7075-1) | 90 tablet | 2024-11-25 | No | No | Historical |