Buspirone Hydrochloride
- Product NDC
- 70518-2300
- 11-digit product format
- 705182300
- Labeler code
- 70518
- Product ID
- 70518-2300_db5d1c23-9c7a-21ca-e053-2995a90a35c9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA204582
- Marketing category
- ANDA
- Marketing start
- 2019-09-05
- Marketing end
- 0000-00-00
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 30 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 |
|---|
| 70518-2300-0 | 70518230000 | 30 TABLET in 1 BLISTER PACK (70518-2300-0) | 30 tablet | 2019-09-05 | 0000-00-00 | No | No | Current |