Buspirone Hydrochloride
- Product NDC
- 50090-5614
- 11-digit product format
- 500905614
- Labeler code
- 50090
- Product ID
- 50090-5614_97b4a6a7-d4fa-499e-aad4-0ed13cf8e4e8
- 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
- 2016-11-14
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 7.5 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Buspirone Hydrochloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BUSPIRONE HYDROCHLORIDE | 7.5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 207LT9J9OC |
| Rxcui | 866111 |
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 |
|---|
| 50090-5614-0 | Buspirone Hydrochloride | 60 in 1 BOTTLE | TABLET | 60 | | 10 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-5614 | BUSPIRONE HYDROCHLORIDE TABLET [A-S MEDICATION SOLUTIONS] | 10 | Current NDC, Legacy NDC, 1 package rows | 20230208_4ae45cb1-8612-4006-b12c-2440160132ac.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 |
|---|
| 50090-5614-0 | 50090561400 | 60 TABLET in 1 BOTTLE (50090-5614-0) | 60 tablet | 2021-08-18 | 0000-00-00 | No | No | Current |