Buspirone Hydrochloride
- Product NDC
- 67046-558
- 11-digit product format
- 670460558
- Labeler code
- 67046
- Product ID
- 67046-558_bc1aa302-c00c-58aa-e053-2995a90a9d2e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Contract Pharmacy Services-PA
- Application
- ANDA204582
- Marketing category
- ANDA
- Marketing start
- 2021-02-01
- Marketing end
- 0000-00-00
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 5 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 |
|---|
| 67046-558-30 | 67046055830 | 30 TABLET in 1 BLISTER PACK (67046-558-30) | 30 tablet | 2021-02-01 | 0000-00-00 | No | No | Current |