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Active Ingredient: IBUPROFEN
Proprietary Name: IBUPROFEN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 400MG
Reference Listed Drug: No
Reference Standard: No
TE Code: Application Number: A071029
Product Number: 001
Approval Date: Mar 23, 1987
Applicant Holder Full Name: HALSEY DRUG CO INC
Marketing Status:
Discontinued
Patent and Exclusivity Information