Active Ingredient: FOLIC ACID
Proprietary Name: FOLIC ACID
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 1MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A088949
Product Number: 001
Approval Date: Sep 13, 1985
Applicant Holder Full Name: PIONEER PHARMACEUTICALS INC
Marketing Status:
Discontinued
Patent and Exclusivity Information