Buspirone HCL
- Product NDC
- 72189-458
- 11-digit product format
- 721890458
- Labeler code
- 72189
- Product ID
- 72189-458_2c4dd247-ae5b-fe93-e063-6394a90a937c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone HCL
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA202330
- Marketing category
- ANDA
- Marketing start
- 2023-03-31
- 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 HCL
- 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#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72189-458-30 | Buspirone HCL | 30 in 1 BOTTLE | TABLET | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72189-458 | BUSPIRONE HCL TABLET [DIRECT_RX] | 2 | Current NDC, 1 package rows | 20250123_f83219c9-8081-fe55-e053-6394a90aa924.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72189-458-30 | 72189045830 | 30 TABLET in 1 BOTTLE (72189-458-30) | 30 tablet | 2023-03-31 | No | No | Current |