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: AB
Application Number: A204575
Product Number: 001
Approval Date: Jun 2, 2016
Applicant Holder Full Name: AUROLIFE PHARMA LLC
Marketing Status:
Prescription
Patent and Exclusivity Information
