# Doxercalciferol

NDC: 71288-802
Generic name: Doxercalciferol
Labeler / Manufacturer: Meitheal Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20200211

FDA application: ANDA211670

## Active ingredients

- DOXERCALCIFEROL: 4 ug/2mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71288-802"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71288-802
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=81a30e4b-be74-41d6-8277-b4f0ea5c15bc