Active Ingredient: HYDROCODONE BITARTRATE; IBUPROFEN
Proprietary Name: VICOPROFEN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 7.5MG;200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N020716
Product Number: 001
Approval Date: Sep 23, 1997
Applicant Holder Full Name: ABBVIE INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
