Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 020135

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MOTRIN (IBUPROFEN)
50MG
Marketing Status: Discontinued

Active Ingredient: IBUPROFEN
Proprietary Name: MOTRIN
Dosage Form; Route of Administration: TABLET, CHEWABLE; ORAL
Strength: 50MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N020135
Product Number: 001
Approval Date: Nov 16, 1994
Applicant Holder Full Name: MCNEIL PEDIATRICS
Marketing Status:  Discontinued
Patent and Exclusivity Information

MOTRIN (IBUPROFEN)
100MG
Marketing Status: Discontinued

Active Ingredient: IBUPROFEN
Proprietary Name: MOTRIN
Dosage Form; Route of Administration: TABLET, CHEWABLE; ORAL
Strength: 100MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N020135
Product Number: 002
Approval Date: Nov 16, 1994
Applicant Holder Full Name: MCNEIL PEDIATRICS
Marketing Status:  Discontinued
Patent and Exclusivity Information