Active Ingredient: IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE
Proprietary Name: IBUPROHM COLD AND SINUS
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 200MG;30MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A074567
Product Number: 001
Approval Date: Apr 17, 2001
Applicant Holder Full Name: OHM LABORATORIES INC
Marketing Status:
Over-the-counter
Patent and Exclusivity Information