Buspirone hydrochloride
- Product NDC
- 42806-665
- 11-digit product format
- 428060665
- Labeler code
- 42806
- Product ID
- 42806-665_ac140e7e-3d5b-4329-8e3e-e21be7417fed
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- EPIC PHARMA, LLC
- Application
- ANDA202087
- Marketing category
- ANDA
- Marketing start
- 2020-06-19
- 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 | 866018, 866083, 866090, 866094 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 42806-665-60 | Buspirone hydrochloride | 60 in 1 BOTTLE | TABLET | 60 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 42806-665 | BUSPIRONE HYDROCHLORIDE TABLET [EPIC PHARMA, LLC] | 3 | Current NDC, Legacy NDC, 1 package rows | 20250109_e8f43c66-f8de-419f-9ea9-43ddc4ec0798.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42806-665-60 | 42806066560 | 60 TABLET in 1 BOTTLE (42806-665-60) | 60 tablet | 2020-06-19 | 0000-00-00 | No | No | Current |