Buspirone Hydrochloride
- Product NDC
- 42291-176
- 11-digit product format
- 422910176
- Labeler code
- 42291
- Product ID
- 42291-176_d57993e3-1dc8-900f-e053-2995a90a6d15
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- buspirone hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AvKARE
- Application
- ANDA075467
- Marketing category
- ANDA
- Marketing start
- 2013-08-29
- Marketing end
- 2022-08-31
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 8 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 42291-176-90 | 42291017690 | 90 TABLET in 1 BOTTLE (42291-176-90) | 90 tablet | 2013-08-29 | 0000-00-00 | No | No | Current |