Buspirone Hydrochloride
- Product NDC
- 58118-0742
- 11-digit product format
- 581180742
- Labeler code
- 58118
- Product ID
- 58118-0742_b0236193-ca9e-2941-e053-2a95a90a03e6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Clinical Solutions Wholesale, LLC
- Application
- ANDA202330
- Marketing category
- ANDA
- Marketing start
- 2018-10-23
- Marketing end
- 0000-00-00
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 58118-0742 | BUSPIRONE HYDROCHLORIDE TABLET [CLINICAL SOLUTIONS WHOLESALE, LLC] | 3 | Legacy NDC | 20200926_dc301942-5119-491f-9e5d-1dd25145e2e4.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 58118-0742-8 | 58118074208 | 30 TABLET in 1 BLISTER PACK (58118-0742-8) | 30 tablet | 2018-10-23 | 0000-00-00 | No | No | Current |