Buspirone Hydrochloride
- Product NDC
- 55700-530
- 11-digit product format
- 557000530
- Labeler code
- 55700
- Product ID
- 55700-530_87e6e57c-7775-4c87-a433-a17377e5bc23
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA202557
- Marketing category
- ANDA
- Marketing start
- 2016-12-15
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-530-30 | 55700053030 | 30 TABLET in 1 BOTTLE (55700-530-30) | 30 tablet | 2017-06-23 | 0000-00-00 | No | No | Current |
| 55700-530-60 | 55700053060 | 60 TABLET in 1 BOTTLE (55700-530-60) | 60 tablet | 2017-06-23 | 0000-00-00 | No | No | Current |