Buspirone Hydrochloride
- Product NDC
- 70518-1924
- 11-digit product format
- 705181924
- Labeler code
- 70518
- Product ID
- 70518-1924_d0fef75c-235a-1757-e053-2a95a90aec0b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA075022
- Marketing category
- ANDA
- Marketing start
- 2019-02-28
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-1924 | BUSPIRONE HYDROCHLORIDE TABLET [REMEDYREPACK INC.] | 6 | Legacy NDC | 20250303_19a8e396-c44f-4533-b9f1-c559e7ab3794.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-1924-1 | 70518192401 | 30 TABLET in 1 BLISTER PACK (70518-1924-1) | 30 tablet | 2021-11-16 | 0000-00-00 | No | No | Current |