Buspirone Hydrochloride
- Product NDC
- 70518-1404
- 11-digit product format
- 705181404
- Labeler code
- 70518
- Product ID
- 70518-1404_e417b0c3-dad6-aeb8-e053-2a95a90ac3f3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA202557
- Marketing category
- ANDA
- Marketing start
- 2018-09-07
- Marketing end
- 0000-00-00
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 5 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 |
|---|
| 70518-1404-0 | 70518140400 | 30 TABLET in 1 BLISTER PACK (70518-1404-0) | 30 tablet | 2018-09-07 | 0000-00-00 | No | No | Current |