DOXERCALCIFEROL
- Product NDC
- 0409-1330
- 11-digit product format
- 004091330
- Labeler code
- 0409
- Product ID
- 0409-1330_08b1cc2b-232b-4f43-b39d-ab2d6de6c3de
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DOXERCALCIFEROL
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Hospira, Inc.
- Application
- NDA208614
- Marketing category
- NDA
- Marketing start
- 2019-10-24
- Marketing end
- 0000-00-00
- Substance
- DOXERCALCIFEROL
- Active strength
- 2 ug/mL
- Pharmacologic classes
- Ergocalciferols [CS],Vitamin D2 Analog [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0409-1330-01 | 00409133001 | 50 VIAL, MULTI-DOSE in 1 CARTON (0409-1330-01) > 2 mL in 1 VIAL, MULTI-DOSE (0409-1330-11) | 2019-10-24 | 0000-00-00 | No | No | Current |