Buspirone Hydrochloride
- Product NDC
- 68071-3240
- 11-digit product format
- 680713240
- Labeler code
- 68071
- Product ID
- 68071-3240_63761d78-ca62-512d-e053-2991aa0ae030
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record