Buspirone Hydrochloride
- Product NDC
- 63629-6818
- 11-digit product format
- 636296818
- Labeler code
- 63629
- Product ID
- 63629-6818_ff1e8ddd-256c-4664-a108-f3e32b524867
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- buspirone hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076008
- Marketing category
- ANDA
- Marketing start
- 2002-03-01
- Marketing end
- 0000-00-00
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 10 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 |
|---|
| 63629-6818-1 | 63629681801 | 60 TABLET in 1 BOTTLE (63629-6818-1) | 60 tablet | 2015-10-15 | 0000-00-00 | No | No | Current |
| 63629-6818-2 | 63629681802 | 90 TABLET in 1 BOTTLE (63629-6818-2) | 90 tablet | 2015-10-15 | 0000-00-00 | No | No | Current |