Buspirone hydrochloride
- Product NDC
- 53217-276
- 11-digit product format
- 532170276
- Labeler code
- 53217
- Product ID
- 53217-276_9c0fa2d3-11b1-4a34-b89a-8a2a9b4bc5ed
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aidarex Pharmaceuticals LLC
- Application
- ANDA078888
- Marketing category
- ANDA
- Marketing start
- 2014-05-03
- Marketing end
- 0000-00-00
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 5 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 53217-276-30 | Buspirone hydrochloride | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
| 53217-276-60 | Buspirone hydrochloride | 60 in 1 BOTTLE | TABLET | 60 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53217-276 | BUSPIRONE HYDROCHLORIDE TABLET [AIDAREX PHARMACEUTICALS LLC] | 1 | Legacy NDC, 2 package rows | 20170420_0efbfbdc-6e9f-4fba-9f2f-e0d948765f9b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 53217-276-30 | 53217027630 | 30 in 1 BOTTLE | Historical |
| 53217-276-60 | 53217027660 | 60 in 1 BOTTLE | Historical |