Buspirone Hydrochloride
- Product NDC
- 68788-7571
- 11-digit product format
- 687887571
- Labeler code
- 68788
- Product ID
- 68788-7571_977fec40-9068-4188-8c45-9a9edae51d7a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA202557
- Marketing category
- ANDA
- Marketing start
- 2016-11-14
- Marketing end
- 0000-00-00
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 8 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 |
|---|
| 68788-7571-1 | 68788757101 | 100 TABLET in 1 BOTTLE (68788-7571-1) | 100 tablet | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7571-3 | 68788757103 | 30 TABLET in 1 BOTTLE (68788-7571-3) | 30 tablet | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7571-6 | 68788757106 | 60 TABLET in 1 BOTTLE (68788-7571-6) | 60 tablet | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7571-9 | 68788757109 | 90 TABLET in 1 BOTTLE (68788-7571-9) | 90 tablet | 2019-12-27 | 0000-00-00 | No | No | Current |