Buspirone Hydrochloride
- Product NDC
- 68788-7885
- 11-digit product format
- 687887885
- Labeler code
- 68788
- Product ID
- 68788-7885_b87b772e-70b2-4cc0-b60b-bf8f8cd5d72e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA202557
- Marketing category
- ANDA
- Marketing start
- 2021-04-16
- Marketing end
- 0000-00-00
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 10 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 |
|---|
| 68788-7885-0 | 68788788500 | 100 TABLET in 1 BOTTLE (68788-7885-0) | 100 tablet | 2021-04-16 | 0000-00-00 | No | No | Current |
| 68788-7885-3 | 68788788503 | 30 TABLET in 1 BOTTLE (68788-7885-3) | 30 tablet | 2021-04-16 | 0000-00-00 | No | No | Current |
| 68788-7885-6 | 68788788506 | 60 TABLET in 1 BOTTLE (68788-7885-6) | 60 tablet | 2021-04-16 | 0000-00-00 | No | No | Current |
| 68788-7885-9 | 68788788509 | 90 TABLET in 1 BOTTLE (68788-7885-9) | 90 tablet | 2021-04-16 | 0000-00-00 | No | No | Current |