Buspirone HCL
- Product NDC
- 72189-628
- 11-digit product format
- 721890628
- Labeler code
- 72189
- Product ID
- 72189-628_37780596-3b70-8d00-e063-6294a90ad4ad
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone HCL
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA210907
- Marketing category
- ANDA
- Marketing start
- 2025-06-13
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 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 HCL
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BUSPIRONE HYDROCHLORIDE | 5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 207LT9J9OC |
| Rxcui | 866094 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72189-628-90 | Buspirone HCL | 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 |
|---|
| 72189-628-90 | 72189062890 | 90 TABLET in 1 BOTTLE (72189-628-90) | 90 tablet | 2025-06-13 | No | No | Current |