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Active Ingredient: IBUPROFEN
Proprietary Name: IBUPROHM
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 400MG
Reference Listed Drug: No
Reference Standard: No
TE Code: Application Number: A070469
Product Number: 001
Approval Date: Aug 29, 1985
Applicant Holder Full Name: OHM LABORATORIES INC.
Marketing Status:
Discontinued
Patent and Exclusivity Information