Active Ingredient: CEFADROXIL/CEFADROXIL HEMIHYDRATE
Proprietary Name: ULTRACEF
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: EQ 500MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A062378
Product Number: 001
Approval Date: Mar 16, 1982
Applicant Holder Full Name: BRISTOL LABORATORIES INC DIV BRISTOL MYERS CO
Marketing Status:
Discontinued
Patent and Exclusivity Information
