Doxercalciferol
- Product NDC
- 0955-1722
- 11-digit product format
- 009551722
- Labeler code
- 0955
- Product ID
- 0955-1722_af718b86-0241-4e8b-9a93-c1933a11636e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxercalciferol
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Winthrop U.S, a business of sanofi-aventis U.S. LLC
- Application
- NDA020862
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2017-04-17
- Marketing end
- 0000-00-00
- Substance
- DOXERCALCIFEROL
- Active strength
- 3 ug/1
- Pharmacologic classes
- Ergocalciferols [CS], Vitamin D2 Analog [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2024-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0955-1722-50 | 00955172250 | 1 BOTTLE in 1 CARTON (0955-1722-50) > 50 CAPSULE in 1 BOTTLE | 1 bottle | 2017-04-17 | 0000-00-00 | No | No | Current |