Buspirone Hydrochloride
- Product NDC
- 50090-5136
- 11-digit product format
- 500905136
- Labeler code
- 50090
- Product ID
- 50090-5136_ef12ed68-f3f6-4f36-964d-15cf6d96b695
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA202557
- Marketing category
- ANDA
- Marketing start
- 2016-12-15
- Marketing end
- 0000-00-00
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 15 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
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 | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5136-1 | 50090513601 | 60 TABLET in 1 BOTTLE (50090-5136-1) | 60 tablet | 2020-08-25 | 0000-00-00 | No | No | Current |
| 50090-5136-3 | 50090513603 | 90 TABLET in 1 BOTTLE (50090-5136-3) | 90 tablet | 2020-08-25 | 0000-00-00 | No | No | Current |