Buspirone Hydrochloride
- Product NDC
- 50090-5405
- 11-digit product format
- 500905405
- Labeler code
- 50090
- Product ID
- 50090-5405_2b8d5ba8-99cf-4902-925f-3431630629ec
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA202330
- Marketing category
- ANDA
- Marketing start
- 2015-06-30
- Marketing end
- 0000-00-00
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 15 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 |
|---|
| 50090-5405-1 | 50090540501 | 60 TABLET in 1 BOTTLE (50090-5405-1) | 60 tablet | 2020-12-09 | 0000-00-00 | No | No | Current |
| 50090-5405-3 | 50090540503 | 90 TABLET in 1 BOTTLE (50090-5405-3) | 90 tablet | 2020-12-09 | 0000-00-00 | No | No | Current |