Buspirone Hydrochloride
- Product NDC
- 63629-8037
- 11-digit product format
- 636298037
- Labeler code
- 63629
- Product ID
- 63629-8037_c64eaa26-14a5-43c0-b9f7-b8544c35ab5c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA202557
- Marketing category
- ANDA
- Marketing start
- 2016-12-15
- Marketing end
- 0000-00-00
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 15 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 63629-8037-1 | 63629803701 | 60 TABLET in 1 BOTTLE (63629-8037-1) | 60 tablet | 2019-07-18 | 0000-00-00 | No | No | Current |