Buspirone Hydrochloride
- Product NDC
- 51407-377
- 11-digit product format
- 514070377
- Labeler code
- 51407
- Product ID
- 51407-377_f1d7848b-b9a3-d3c5-e053-2a95a90a2658
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA202330
- Marketing category
- ANDA
- Marketing start
- 2014-08-25
- Marketing end
- 2023-03-31
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 30 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 51407-377-60 | 51407037760 | 60 TABLET in 1 BOTTLE (51407-377-60) | 60 tablet | 2020-06-18 | 0000-00-00 | No | No | Current |