Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 077660

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ESCITALOPRAM OXALATE (ESCITALOPRAM OXALATE)
EQ 5MG BASE
Marketing Status: Discontinued

Active Ingredient: ESCITALOPRAM OXALATE
Proprietary Name: ESCITALOPRAM OXALATE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: EQ 5MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A077660
Product Number: 001
Approval Date: Jul 31, 2007
Applicant Holder Full Name: MYLAN PHARMACEUTICALS INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

ESCITALOPRAM OXALATE (ESCITALOPRAM OXALATE)
EQ 10MG BASE
Marketing Status: Discontinued

Active Ingredient: ESCITALOPRAM OXALATE
Proprietary Name: ESCITALOPRAM OXALATE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: EQ 10MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A077660
Product Number: 002
Approval Date: Jul 31, 2007
Applicant Holder Full Name: MYLAN PHARMACEUTICALS INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

ESCITALOPRAM OXALATE (ESCITALOPRAM OXALATE)
EQ 20MG BASE
Marketing Status: Discontinued

Active Ingredient: ESCITALOPRAM OXALATE
Proprietary Name: ESCITALOPRAM OXALATE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: EQ 20MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A077660
Product Number: 003
Approval Date: Jul 31, 2007
Applicant Holder Full Name: MYLAN PHARMACEUTICALS INC
Marketing Status:  Discontinued
Patent and Exclusivity Information