Buspirone hydrochloride
- Product NDC
- 66267-875
- 11-digit product format
- 662670875
- Labeler code
- 66267
- Product ID
- 66267-875_9caf8590-f761-c959-e053-2995a90ab836
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA078888
- Marketing category
- ANDA
- Marketing start
- 2014-05-03
- Marketing end
- 0000-00-00
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 15 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record