Buspirone Hydrochloride
- Product NDC
- 42291-177
- 11-digit product format
- 422910177
- Labeler code
- 42291
- Product ID
- 42291-177_d579db86-b5cf-a3b4-e053-2995a90ad23b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AvKARE
- Application
- ANDA075022
- Marketing category
- ANDA
- Marketing start
- 2013-10-17
- Marketing end
- 0000-00-00
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 30 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42291-177-50 | 42291017750 | 500 TABLET in 1 BOTTLE (42291-177-50) | 500 tablet | 2013-10-17 | 0000-00-00 | No | No | Current |