Active Ingredient: CEFADROXIL/CEFADROXIL HEMIHYDRATE
Proprietary Name: DURICEF
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: EQ 500MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N050512
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: WARNER CHILCOTT INC
Marketing Status:
Discontinued
Patent and Exclusivity Information