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Active Ingredient: DOXERCALCIFEROL
Proprietary Name: DOXERCALCIFEROL
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 4MCG/2ML (2MCG/ML)
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A200926
Product Number: 001
Approval Date: Feb 4, 2014
Applicant Holder Full Name: SANDOZ INC
Marketing Status:
Prescription
Patent and Exclusivity Information
