Buspirone Hydrochloride
- Product NDC
- 71610-267
- 11-digit product format
- 716100267
- Labeler code
- 71610
- Product ID
- 71610-267_52da6ae2-944a-4609-a3a0-07cfb06b31a2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA204582
- Marketing category
- ANDA
- Marketing start
- 2012-06-29
- Marketing end
- 0000-00-00
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 5 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71610-267 | BUSPIRONE HYDROCHLORIDE TABLET [APHENA PHARMA SOLUTIONS - TENNESSEE, LLC] | 1 | Legacy NDC | 20190515_b2266389-ab0f-484e-8099-4eaa19ac18c3.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71610-267-53 | 71610026753 | 60 TABLET in 1 BOTTLE (71610-267-53) | 60 tablet | 2019-05-01 | 0000-00-00 | No | No | Current |
| 71610-267-60 | 71610026760 | 90 TABLET in 1 BOTTLE (71610-267-60) | 90 tablet | 2019-05-01 | 0000-00-00 | No | No | Current |
| 71610-267-80 | 71610026780 | 180 TABLET in 1 BOTTLE (71610-267-80) | 180 tablet | 2019-05-01 | 0000-00-00 | No | No | Current |