Active Ingredient: HYDROCODONE BITARTRATE; IBUPROFEN
Proprietary Name: HYDROCODONE BITARTRATE AND IBUPROFEN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 7.5MG;200MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A076023
Product Number: 001
Approval Date: Apr 11, 2003
Applicant Holder Full Name: TEVA PHARMACEUTICALS USA INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
