Buspirone Hydrochloride
- Product NDC
- 70518-3091
- 11-digit product format
- 705183091
- Labeler code
- 70518
- Product ID
- 70518-3091_eb3be630-4fe3-723d-e053-2a95a90a6b71
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA210907
- Marketing category
- ANDA
- Marketing start
- 2021-05-10
- Marketing end
- 0000-00-00
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 15 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 70518-3091 | BUSPIRONE HYDROCHLORIDE TABLET [REMEDYREPACK INC.] | 5 | Legacy NDC | 20240314_81e27c70-fb19-4533-8a6c-8aa00e20f667.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3091-0 | 70518309100 | 30 TABLET in 1 BLISTER PACK (70518-3091-0) | 30 tablet | 2021-05-10 | 0000-00-00 | No | No | Current |
| 70518-3091-1 | 70518309101 | 60 TABLET in 1 BOTTLE, PLASTIC (70518-3091-1) | 60 tablet | 2021-07-23 | 0000-00-00 | No | No | Current |