Buspirone hydrochloride
- Product NDC
- 72162-2199
- 11-digit product format
- 721622199
- Labeler code
- 72162
- Product ID
- 72162-2199_9215bf81-1137-4e26-989d-a52124afbff9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA078888
- Marketing category
- ANDA
- Marketing start
- 2023-03-21
- 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#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-2199-1 | Buspirone hydrochloride | 100 in 1 BOTTLE | TABLET | 100 | | 101 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-2199 | BUSPIRONE HYDROCHLORIDE TABLET [BRYANT RANCH PREPACK] | 101 | Current NDC, 1 package rows | 20241116_b07c0a91-892c-47f5-819e-a128e0ef1ed7.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 |
|---|
| 72162-2199-1 | 72162219901 | 100 TABLET in 1 BOTTLE (72162-2199-1) | 100 tablet | 2023-12-15 | No | No | Historical |