Buspirone Hydrochloride
- Product NDC
- 71335-2150
- 11-digit product format
- 713352150
- Labeler code
- 71335
- Product ID
- 71335-2150_20a55442-3cef-4b55-8830-7f6cb18ff58d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- buspirone hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076008
- Marketing category
- ANDA
- Marketing start
- 2013-07-08
- Marketing end
- 0000-00-00
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 8 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 |
|---|
| 71335-2150 | BUSPIRONE HYDROCHLORIDE TABLET [BRYANT RANCH PREPACK] | 101 | Legacy NDC | 20231206_5c7288bf-45a9-424b-ac39-dcdf05400bfb.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-2150-1 | 71335215001 | 30 TABLET in 1 BOTTLE, PLASTIC (71335-2150-1) | 30 tablet | 2022-08-22 | 0000-00-00 | No | No | Current |
| 71335-2150-2 | 71335215002 | 90 TABLET in 1 BOTTLE, PLASTIC (71335-2150-2) | 90 tablet | 2022-08-22 | 0000-00-00 | No | No | Current |
| 71335-2150-3 | 71335215003 | 18 TABLET in 1 BOTTLE, PLASTIC (71335-2150-3) | 18 tablet | 2022-08-22 | 0000-00-00 | No | No | Current |
| 71335-2150-4 | 71335215004 | 28 TABLET in 1 BOTTLE, PLASTIC (71335-2150-4) | 28 tablet | 2022-08-22 | 0000-00-00 | No | No | Current |
| 71335-2150-5 | 71335215005 | 60 TABLET in 1 BOTTLE, PLASTIC (71335-2150-5) | 60 tablet | 2022-08-22 | 0000-00-00 | No | No | Current |
| 71335-2150-6 | 71335215006 | 120 TABLET in 1 BOTTLE, PLASTIC (71335-2150-6) | 120 tablet | 2022-08-22 | 0000-00-00 | No | No | Current |