Buspirone Hydrochloride
- Product NDC
- 50090-3260
- 11-digit product format
- 500903260
- Labeler code
- 50090
- Product ID
- 50090-3260_5a916f59-29ed-4628-8e09-cdf7fa1830ec
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- 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
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 |
|---|
| 50090-3260-0 | 50090326000 | 30 TABLET in 1 BOTTLE (50090-3260-0) | 30 tablet | 2017-11-16 | 0000-00-00 | No | No | Current |
| 50090-3260-1 | 50090326001 | 90 TABLET in 1 BOTTLE (50090-3260-1) | 90 tablet | 2017-11-14 | 0000-00-00 | No | No | Current |
| 50090-3260-3 | 50090326003 | 180 TABLET in 1 BOTTLE (50090-3260-3) | 180 tablet | 2017-11-29 | 0000-00-00 | No | No | Current |
| 50090-3260-4 | 50090326004 | 45 TABLET in 1 BOTTLE (50090-3260-4) | 45 tablet | 2017-11-24 | 0000-00-00 | No | No | Current |
| 50090-3260-5 | 50090326005 | 60 TABLET in 1 BOTTLE (50090-3260-5) | 60 tablet | 2017-11-16 | 0000-00-00 | No | No | Current |