Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 200882

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ESOMEPRAZOLE SODIUM (ESOMEPRAZOLE SODIUM)
EQ 40MG BASE/VIAL
Marketing Status: Prescription

Active Ingredient: ESOMEPRAZOLE SODIUM
Proprietary Name: ESOMEPRAZOLE SODIUM
Dosage Form; Route of Administration: INJECTABLE; INTRAVENOUS
Strength: EQ 40MG BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A200882
Product Number: 002
Approval Date: Mar 18, 2013
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status:  Prescription
Patent and Exclusivity Information

ESOMEPRAZOLE SODIUM (ESOMEPRAZOLE SODIUM)
EQ 20MG BASE/VIAL
Marketing Status: Discontinued

Active Ingredient: ESOMEPRAZOLE SODIUM
Proprietary Name: ESOMEPRAZOLE SODIUM
Dosage Form; Route of Administration: INJECTABLE; INTRAVENOUS
Strength: EQ 20MG BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A200882
Product Number: 001
Approval Date: Mar 18, 2013
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status:  Discontinued
Patent and Exclusivity Information