Doxercalciferol
- Product NDC
- 0781-3305
- 11-digit product format
- 007813305
- Labeler code
- 0781
- Product ID
- 0781-3305_ff1d9e28-4bb1-485b-b860-446e715019fb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxercalciferol
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Sandoz Inc
- Application
- ANDA200926
- Marketing category
- ANDA
- Marketing start
- 2014-02-04
- Marketing end
- 0000-00-00
- Substance
- DOXERCALCIFEROL
- Active strength
- 4 ug/2mL
- Pharmacologic classes
- Ergocalciferols [CS],Vitamin D2 Analog [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record