Buspirone Hydrochloride
- Product NDC
- 45865-887
- 11-digit product format
- 458650887
- Labeler code
- 45865
- Product ID
- 45865-887_7dc7c367-1d74-7634-e053-2a91aa0a9cb9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- medsource pharmaceuticals
- Application
- ANDA075022
- Marketing category
- ANDA
- Marketing start
- 2002-03-01
- Marketing end
- 0000-00-00
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 15 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 |
|---|
| 45865-887-30 | Buspirone Hydrochloride | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 45865-887 | BUSPIRONE HYDROCHLORIDE TABLET [MEDSOURCE PHARMACEUTICALS] | 1 | Legacy NDC, 1 package rows | 20181225_7dc7c367-1d73-7634-e053-2a91aa0a9cb9.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 45865-887-30 | 45865088730 | 30 in 1 BOTTLE | Historical |