Buspirone hydrochloride
- Product NDC
- 0904-6899
- 11-digit product format
- 009046899
- Labeler code
- 0904
- Product ID
- 0904-6899_88587ddd-72d8-4312-8619-e78e2393cdb6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA078888
- Marketing category
- ANDA
- Marketing start
- 2014-05-03
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 15 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 | 15 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 207LT9J9OC |
| Rxcui | 866018 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0904-6899-61 | Buspirone hydrochloride | 1 in 1 BLISTER PACK | TABLET | 1 | | 9 |
| 0904-6899-61 | Buspirone hydrochloride | 100 in 1 CARTON | TABLET | 100 | | 9 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0904-6899 | BUSPIRONE HYDROCHLORIDE TABLET [MAJOR PHARMACEUTICALS] | 8 | Current NDC, Legacy NDC, 2 package rows | 20250410_a9bb9216-3dac-4e8a-9df9-f72c2eaef160.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 |
|---|
| 0904-6899-61 | 00904689961 | 100 BLISTER PACK in 1 CARTON (0904-6899-61) / 1 TABLET in 1 BLISTER PACK | 100 blister pack | 2014-05-03 | 0000-00-00 | No | No | Current |