BUSPIRONE HYDROCHLORIDE
- Product NDC
- 50090-7075
- 11-digit product format
- 500907075
- Labeler code
- 50090
- Product ID
- 50090-7075_ddd3d399-ddda-4d53-8fc5-a27e71b21b49
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- BUSPIRONE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA078246
- Marketing category
- ANDA
- Marketing start
- 2020-02-21
- 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 |
|---|
| 50090-7075-0 | BUSPIRONE HYDROCHLORIDE | 60 in 1 BOTTLE | TABLET | 60 | | 7 |
| 50090-7075-1 | BUSPIRONE HYDROCHLORIDE | 90 in 1 BOTTLE | TABLET | 90 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-7075 | BUSPIRONE HYDROCHLORIDE TABLET [A-S MEDICATION SOLUTIONS] | 7 | Current NDC, 2 package rows | 20241205_529ab1f9-534c-4a45-aa70-76e605247af1.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 |
|---|
| 50090-7075-0 | 50090707500 | 60 TABLET in 1 BOTTLE (50090-7075-0) | 60 tablet | 2024-01-25 | No | No | Current |
| 50090-7075-1 | 50090707501 | 90 TABLET in 1 BOTTLE (50090-7075-1) | 90 tablet | 2024-11-25 | No | No | Current |