Buspirone Hydrochloride
- Product NDC
- 50090-7742
- 11-digit product format
- 500907742
- Labeler code
- 50090
- Product ID
- 50090-7742_61f62c95-086e-451e-a2c1-9e286a4a0e88
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- buspirone hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA078302
- Marketing category
- ANDA
- Marketing start
- 2020-05-01
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 30 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 | 30 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 207LT9J9OC |
| Rxcui | 866090 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-7742-0 | Buspirone Hydrochloride | 60 in 1 BOTTLE | TABLET | 60 | | 1 |
| 50090-7742-1 | Buspirone Hydrochloride | 90 in 1 BOTTLE | TABLET | 90 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7742-0 | 50090774200 | 60 TABLET in 1 BOTTLE (50090-7742-0) | 60 tablet | 2025-10-29 | No | No | Current |
| 50090-7742-1 | 50090774201 | 90 TABLET in 1 BOTTLE (50090-7742-1) | 90 tablet | 2025-10-29 | No | No | Current |