Buspirone Hydrochloride
- Product NDC
- 63629-6817
- 11-digit product format
- 636296817
- Labeler code
- 63629
- Product ID
- 63629-6817_b78e94b4-3fdd-4b4d-800f-290d7ed6611c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- buspirone hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA075467
- Marketing category
- ANDA
- Marketing start
- 2012-04-23
- Marketing end
- 0000-00-00
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 8 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-6817-1 | 63629681701 | 30 TABLET in 1 BOTTLE (63629-6817-1) | 30 tablet | 2015-10-16 | 0000-00-00 | No | No | Current |
| 63629-6817-2 | 63629681702 | 60 TABLET in 1 BOTTLE (63629-6817-2) | 60 tablet | 2015-10-16 | 0000-00-00 | No | No | Current |