Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 077795

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OXCARBAZEPINE (OXCARBAZEPINE)
150MG
Marketing Status: Discontinued

Active Ingredient: OXCARBAZEPINE
Proprietary Name: OXCARBAZEPINE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 150MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A077795
Product Number: 001
Approval Date: Oct 9, 2007
Applicant Holder Full Name: HIKMA PHARMACEUTICALS USA INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

OXCARBAZEPINE (OXCARBAZEPINE)
300MG
Marketing Status: Discontinued

Active Ingredient: OXCARBAZEPINE
Proprietary Name: OXCARBAZEPINE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 300MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A077795
Product Number: 002
Approval Date: Oct 9, 2007
Applicant Holder Full Name: HIKMA PHARMACEUTICALS USA INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

OXCARBAZEPINE (OXCARBAZEPINE)
600MG
Marketing Status: Discontinued

Active Ingredient: OXCARBAZEPINE
Proprietary Name: OXCARBAZEPINE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 600MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A077795
Product Number: 003
Approval Date: Oct 9, 2007
Applicant Holder Full Name: HIKMA PHARMACEUTICALS USA INC
Marketing Status:  Discontinued
Patent and Exclusivity Information