Active Ingredient: FOLIC ACID
Proprietary Name: FOLIC ACID
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N006135
Product Number: 003
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ELI LILLY AND CO
Marketing Status:
Discontinued
Patent and Exclusivity Information