Buspirone Hydrochloride
- Product NDC
- 50090-2998
- 11-digit product format
- 500902998
- Labeler code
- 50090
- Product ID
- 50090-2998_a4abe526-af9d-441b-a12e-a64ab11cbf9a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- buspirone hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA076008
- Marketing category
- ANDA
- Marketing start
- 2002-03-01
- Marketing end
- 0000-00-00
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 5 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 50090-2998-0 | Buspirone Hydrochloride | 33 in 1 CARTON | TABLET | 33 | | 17 |
| 50090-2998-0 | Buspirone Hydrochloride | 1 in 1 BLISTER PACK | TABLET | 1 | | 17 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2998 | BUSPIRONE HYDROCHLORIDE TABLET [A-S MEDICATION SOLUTIONS] | 17 | Legacy NDC, 2 package rows | 20180821_597d668d-5f9b-4a51-8145-14e4dcc1f6c7.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50090-2998-0 | 50090299800 | 33 in 1 CARTON | Historical |