busPIRone HCl
- Product NDC
- 69238-1117
- 11-digit product format
- 692381117
- Labeler code
- 69238
- Product ID
- 69238-1117_f697167a-4d7c-42fb-91c0-7c1f877bf54a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- buspirone hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Amneal Pharmaceuticals NY LLC
- Application
- ANDA208829
- Marketing category
- ANDA
- Marketing start
- 2017-05-24
- 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 |
|---|
| 69238-1117 | BUSPIRONE HCL (BUSPIRONE HYDROCHLORIDE) TABLET [AMNEAL PHARMACEUTICALS NY LLC] | 8 | Legacy NDC | 20241205_33999f17-f689-40a1-955a-fb19c0590e0e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69238-1117-1 | 69238111701 | 100 TABLET in 1 BOTTLE (69238-1117-1) | 100 tablet | 2017-05-24 | 0000-00-00 | No | No | Current |
| 69238-1117-5 | 69238111705 | 500 TABLET in 1 BOTTLE (69238-1117-5) | 500 tablet | 2017-05-24 | 0000-00-00 | No | No | Current |