Buspirone Hydrochloride
- Product NDC
- 50090-4182
- 11-digit product format
- 500904182
- Labeler code
- 50090
- Product ID
- 50090-4182_b4d23538-4d7c-43e9-baca-5bc3aa40974d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA075022
- Marketing category
- ANDA
- Marketing start
- 2002-02-28
- Marketing end
- 0000-00-00
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2024-12-31
- 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 |
|---|
| 50090-4182-0 | 50090418200 | 30 TABLET in 1 BOTTLE (50090-4182-0) | 30 tablet | 2019-10-09 | 0000-00-00 | No | No | Current |
| 50090-4182-1 | 50090418201 | 90 TABLET in 1 BOTTLE (50090-4182-1) | 90 tablet | 2019-10-09 | 0000-00-00 | No | No | Current |
| 50090-4182-2 | 50090418202 | 100 TABLET in 1 BOTTLE (50090-4182-2) | 100 tablet | 2019-10-09 | 0000-00-00 | No | No | Current |
| 50090-4182-3 | 50090418203 | 180 TABLET in 1 BOTTLE (50090-4182-3) | 180 tablet | 2019-10-09 | 0000-00-00 | No | No | Current |
| 50090-4182-4 | 50090418204 | 45 TABLET in 1 BOTTLE (50090-4182-4) | 45 tablet | 2019-10-09 | 0000-00-00 | No | No | Current |
| 50090-4182-5 | 50090418205 | 60 TABLET in 1 BOTTLE (50090-4182-5) | 60 tablet | 2019-03-12 | 0000-00-00 | No | No | Current |