Buspirone hydrochloride
- Product NDC
- 68788-6878
- 11-digit product format
- 687886878
- Labeler code
- 68788
- Product ID
- 68788-6878_6810d613-9f1d-43bd-82a7-c6f39b67704a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA078888
- Marketing category
- ANDA
- Marketing start
- 2017-01-23
- Marketing end
- 0000-00-00
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 5 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 68788-6878-1 | 68788687801 | 100 TABLET in 1 BOTTLE (68788-6878-1) | 100 tablet | 2017-01-23 | 0000-00-00 | No | No | Current |
| 68788-6878-3 | 68788687803 | 30 TABLET in 1 BOTTLE (68788-6878-3) | 30 tablet | 2017-01-23 | 0000-00-00 | No | No | Current |
| 68788-6878-6 | 68788687806 | 60 TABLET in 1 BOTTLE (68788-6878-6) | 60 tablet | 2017-01-23 | 0000-00-00 | No | No | Current |
| 68788-6878-9 | 68788687809 | 90 TABLET in 1 BOTTLE (68788-6878-9) | 90 tablet | 2017-01-23 | 0000-00-00 | No | No | Current |