Active Ingredient: ASCORBIC ACID
Proprietary Name: ASCOR
Dosage Form; Route of Administration: SOLUTION; INTRAVENOUS
Strength: 25,000MG/50ML (500MG/ML)
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code:
Application Number: N209112
Product Number: 001
Approval Date: Oct 2, 2017
Applicant Holder Full Name: MCGUFF PHARMACEUTICALS INC
Marketing Status:
Prescription
Patent and Exclusivity Information
