Buspirone hydrochloride
- Product NDC
- 50090-2111
- 11-digit product format
- 500902111
- Labeler code
- 50090
- Product ID
- 50090-2111_3e2b9759-e55f-481e-81c8-118a4d96de23
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA078888
- Marketing category
- ANDA
- Marketing start
- 2014-05-03
- Marketing end
- 0000-00-00
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 15 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-2111-1 | Buspirone hydrochloride | 60 in 1 BOTTLE | TABLET | 60 | | 15 |
| 50090-2111-3 | Buspirone hydrochloride | 90 in 1 BOTTLE | TABLET | 90 | | 15 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2111 | BUSPIRONE HYDROCHLORIDE TABLET [A-S MEDICATION SOLUTIONS] | 15 | Legacy NDC, 2 package rows | 20210310_58c72553-d118-4275-8427-d3ffb886911b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-2111-1 | 50090211101 | 60 TABLET in 1 BOTTLE (50090-2111-1) | 60 tablet | 2015-10-14 | 0000-00-00 | No | No | Current |
| 50090-2111-3 | 50090211103 | 90 TABLET in 1 BOTTLE (50090-2111-3) | 90 tablet | 2018-03-12 | 0000-00-00 | No | No | Current |