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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 074035

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KETOPROFEN (KETOPROFEN)
50MG
Marketing Status: Discontinued
Active Ingredient: KETOPROFEN
Proprietary Name: KETOPROFEN
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 50MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A074035
Product Number: 002
Approval Date: Dec 31, 1996
Applicant Holder Full Name: RISING PHARMA HOLDING INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
KETOPROFEN (KETOPROFEN)
75MG
Marketing Status: Discontinued
Active Ingredient: KETOPROFEN
Proprietary Name: KETOPROFEN
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 75MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A074035
Product Number: 003
Approval Date: Dec 31, 1996
Applicant Holder Full Name: RISING PHARMA HOLDING INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
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