Active Ingredient: IBUPROFEN; PHENYLEPHRINE HYDROCHLORIDE
Proprietary Name: IBUPROFEN AND PHENYLEPHRINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 200MG;10MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A203200
Product Number: 001
Approval Date: Jul 3, 2014
Applicant Holder Full Name: PERRIGO R AND D CO
Marketing Status:
Over-the-counter
Patent and Exclusivity Information
