Buspirone Hydrochloride
- Product NDC
- 70518-1747
- 11-digit product format
- 705181747
- Labeler code
- 70518
- Product ID
- 70518-1747_dfc2c37b-7805-659a-e053-2a95a90a214d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA075022
- Marketing category
- ANDA
- Marketing start
- 2018-12-21
- Marketing end
- 0000-00-00
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 10 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 |
|---|
| 70518-1747 | BUSPIRONE HYDROCHLORIDE TABLET [REMEDYREPACK INC.] | 10 | Legacy NDC | 20250228_974c3e79-6bb5-42ad-ab65-143f3c7f4d66.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-1747-0 | 70518174700 | 30 TABLET in 1 BLISTER PACK (70518-1747-0) | 30 tablet | 2018-12-21 | 0000-00-00 | No | No | Current |