Buspirone hydrochloride
- Product NDC
- 55700-526
- 11-digit product format
- 557000526
- Labeler code
- 55700
- Product ID
- 55700-526_a645cabe-dd43-452c-b93f-6e3d42058ed3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA078888
- Marketing category
- ANDA
- Marketing start
- 2014-05-03
- Marketing end
- 0000-00-00
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 10 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 |
|---|
| 55700-526-30 | 55700052630 | 30 TABLET in 1 BOTTLE (55700-526-30) | 30 tablet | 2017-06-02 | 0000-00-00 | No | No | Current |
| 55700-526-90 | 55700052690 | 90 TABLET in 1 BOTTLE (55700-526-90) | 90 tablet | 2019-12-06 | 0000-00-00 | No | No | Current |