Buspirone Hydrochloride
- Product NDC
- 63629-3333
- 11-digit product format
- 636293333
- Labeler code
- 63629
- Product ID
- 63629-3333_35775dd8-6973-41ab-b1ee-f8b7c1fabb31
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA075022
- Marketing category
- ANDA
- Marketing start
- 2004-03-26
- Marketing end
- 0000-00-00
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 30 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 |
|---|
| 63629-3333-1 | 63629333301 | 60 TABLET in 1 BOTTLE (63629-3333-1) | 60 tablet | 2009-02-05 | 0000-00-00 | No | No | Current |
| 63629-3333-2 | 63629333302 | 30 TABLET in 1 BOTTLE (63629-3333-2) | 30 tablet | 2009-02-05 | 0000-00-00 | No | No | Current |
| 63629-3333-3 | 63629333303 | 56 TABLET in 1 BOTTLE (63629-3333-3) | 56 tablet | 2009-02-05 | 0000-00-00 | No | No | Current |
| 63629-3333-4 | 63629333304 | 90 TABLET in 1 BOTTLE (63629-3333-4) | 90 tablet | 2009-02-05 | 0000-00-00 | No | No | Current |
| 63629-3333-5 | 63629333305 | 180 TABLET in 1 BOTTLE (63629-3333-5) | 180 tablet | 2009-02-05 | 0000-00-00 | No | No | Current |
| 63629-3333-6 | 63629333306 | 15 TABLET in 1 BOTTLE (63629-3333-6) | 15 tablet | 2009-02-05 | 0000-00-00 | No | No | Current |