Buspirone Hydrochloride
- Product NDC
- 49999-812
- 11-digit product format
- 499990812
- Labeler code
- 49999
- Product ID
- 49999-812_4245ef47-4a3e-46b9-a532-40ae32f4ffdb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA074253
- Marketing category
- ANDA
- Marketing start
- 2010-11-16
- Marketing end
- 0000-00-00
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record