Buspirone Hydrochloride
- Product NDC
- 55700-881
- 11-digit product format
- 557000881
- Labeler code
- 55700
- Product ID
- 55700-881_ec9c9068-b183-47ee-9e2b-c91739e68dab
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA208972
- Marketing category
- ANDA
- Marketing start
- 2020-09-03
- Marketing end
- 0000-00-00
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 8 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-881-30 | 55700088130 | 30 TABLET in 1 BOTTLE (55700-881-30) | 30 tablet | 2020-09-03 | 0000-00-00 | No | No | Current |