Active Ingredient: CEFDINIR
Proprietary Name: OMNICEF
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N050739
Product Number: 001
Approval Date: Dec 4, 1997
Applicant Holder Full Name: ABBVIE INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
