Buspirone hydrochloride
- Product NDC
- 70518-1050
- 11-digit product format
- 705181050
- Labeler code
- 70518
- Product ID
- 70518-1050_e2bfd5ec-b5b2-cd08-e053-2995a90aeaca
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA078888
- Marketing category
- ANDA
- Marketing start
- 2018-03-01
- Marketing end
- 0000-00-00
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 15 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 70518-1050-1 | 70518105001 | 60 TABLET in 1 BLISTER PACK (70518-1050-1) | 60 tablet | 2021-05-05 | 0000-00-00 | No | No | Current |