Buspirone Hydrochloride
- Product NDC
- 50436-2010
- 11-digit product format
- 504362010
- Labeler code
- 50436
- Product ID
- 50436-2010_93d3808b-cd46-461e-93ea-af906778efae
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA202557
- Marketing category
- ANDA
- Marketing start
- 2016-11-14
- Marketing end
- 0000-00-00
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 8 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 50436-2010-1 | Buspirone Hydrochloride | 30 in 1 BOTTLE | TABLET | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-2010 | BUSPIRONE HYDROCHLORIDE TABLET [UNIT DOSE SERVICES] | 2 | Legacy NDC, 1 package rows | 20190921_f6524d3a-a98c-416f-a2c4-869050de5158.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50436-2010-1 | 50436201001 | 30 in 1 BOTTLE | Historical |