Buspirone Hydrochloride
- Product NDC
- 51407-417
- 11-digit product format
- 514070417
- Labeler code
- 51407
- Product ID
- 51407-417_4b1f20ca-5708-e1f4-e063-6294a90ac5dc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA202330
- Marketing category
- ANDA
- Marketing start
- 2014-08-25
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 30 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Buspirone Hydrochloride
- Listing expiration
- 2027-12-31
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, 866111 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51407-417-60 | Buspirone Hydrochloride | 60 in 1 BOTTLE | TABLET | 60 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51407-417 | BUSPIRONE HYDROCHLORIDE TABLET [GOLDEN STATE MEDICAL SUPPLY, INC.] | 5 | Current NDC, Legacy NDC, 1 package rows | 20240823_bcce49d3-c8eb-9f9b-e053-2995a90a67d9.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 |
|---|
| 51407-417-60 | 51407041760 | 60 TABLET in 1 BOTTLE (51407-417-60) | 60 tablet | 2021-04-01 | 0000-00-00 | No | No | Current |