Buspirone Hydrochloride
- Product NDC
- 67046-349
- 11-digit product format
- 670460349
- Labeler code
- 67046
- Product ID
- 67046-349_a82b99f2-c056-093c-e053-2a95a90ace65
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Contract Pharmacy Services-PA
- Application
- ANDA202557
- Marketing category
- ANDA
- Marketing start
- 2020-06-15
- Marketing end
- 0000-00-00
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 8 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 67046-349-30 | Buspirone Hydrochloride | 30 in 1 BLISTER PACK | TABLET | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67046-349 | BUSPIRONE HYDROCHLORIDE TABLET [CONTRACT PHARMACY SERVICES-PA] | 1 | Legacy NDC, 1 package rows | 20200618_a82b9a81-700f-81e1-e053-2a95a90aeb2a.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 |
|---|
| 67046-349-30 | 67046034930 | 30 TABLET in 1 BLISTER PACK (67046-349-30) | 30 tablet | 2020-06-15 | 0000-00-00 | No | No | Current |