Buspirone HCl
- Product NDC
- 53808-0856
- 11-digit product format
- 538080856
- Labeler code
- 53808
- Product ID
- 53808-0856_db45c4b3-9d13-44dd-9b8d-b2ae6a2c4c36
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- State of Florida DOH Central Pharmacy
- Application
- ANDA074253
- Marketing category
- ANDA
- Marketing start
- 2013-01-01
- Marketing end
- 0000-00-00
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 10 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 |
|---|
| 53808-0856-1 | Buspirone HCl | 30 in 1 BLISTER PACK | TABLET | 30 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53808-0856 | BUSPIRONE HCL (BUSPIRONE HYDROCHLORIDE) TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 5 | Legacy NDC, 1 package rows | 20141020_f61184d1-e34a-4a84-9432-a7bacf09e818.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 53808-0856-1 | 53808085601 | 30 in 1 BLISTER PACK | Historical |