Buspirone Hydrochloride
- Product NDC
- 68788-6984
- 11-digit product format
- 687886984
- Labeler code
- 68788
- Product ID
- 68788-6984_7f2c9b31-a42a-49ff-bd20-1d59004c7e54
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA202557
- Marketing category
- ANDA
- Marketing start
- 2017-07-05
- Marketing end
- 0000-00-00
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 5 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 |
|---|
| 68788-6984-1 | 68788698401 | 100 TABLET in 1 BOTTLE (68788-6984-1) | 100 tablet | 2017-07-05 | 0000-00-00 | No | No | Current |
| 68788-6984-3 | 68788698403 | 30 TABLET in 1 BOTTLE (68788-6984-3) | 30 tablet | 2017-07-05 | 0000-00-00 | No | No | Current |
| 68788-6984-6 | 68788698406 | 60 TABLET in 1 BOTTLE (68788-6984-6) | 60 tablet | 2017-07-05 | 0000-00-00 | No | No | Current |
| 68788-6984-9 | 68788698409 | 90 TABLET in 1 BOTTLE (68788-6984-9) | 90 tablet | 2017-07-05 | 0000-00-00 | No | No | Current |