Buspirone Hydrochloride
- Product NDC
- 50090-3168
- 11-digit product format
- 500903168
- Labeler code
- 50090
- Product ID
- 50090-3168_8b45a6c6-14f5-4e7e-af6f-83372fcd3a71
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA202557
- Marketing category
- ANDA
- Marketing start
- 2016-12-15
- Marketing end
- 0000-00-00
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 10 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 |
|---|
| 50090-3168-0 | Buspirone Hydrochloride | 33 in 1 BOTTLE | TABLET | 33 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-3168 | BUSPIRONE HYDROCHLORIDE TABLET [A-S MEDICATION SOLUTIONS] | 4 | Legacy NDC, 1 package rows | 20210303_15bc08bf-d3b4-4498-b488-cec0a428d278.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 |
|---|
| 50090-3168-0 | 50090316800 | 33 TABLET in 1 BOTTLE (50090-3168-0) | 33 tablet | 2017-10-13 | 0000-00-00 | No | No | Current |