Buspirone Hydrochloride
- Product NDC
- 55700-937
- 11-digit product format
- 557000937
- Labeler code
- 55700
- Product ID
- 55700-937_ee4ef576-1c41-4fce-9196-2e7ec3d4103b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA202330
- Marketing category
- ANDA
- Marketing start
- 2021-09-14
- 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 |
|---|
| 55700-937-30 | 55700093730 | 30 TABLET in 1 BOTTLE (55700-937-30) | 30 tablet | 2021-09-14 | 0000-00-00 | No | No | Current |