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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 211908

ZIPRASIDONE MESYLATE (ZIPRASIDONE MESYLATE)
EQ 20MG BASE/VIAL
Marketing Status: Prescription
Active Ingredient: ZIPRASIDONE MESYLATE
Proprietary Name: ZIPRASIDONE MESYLATE
Dosage Form; Route of Administration: POWDER; INTRAMUSCULAR
Strength: EQ 20MG BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A211908
Product Number: 001
Approval Date: Dec 26, 2019
Applicant Holder Full Name: GLAND PHARMA LTD
Marketing Status:  Prescription
Patent and Exclusivity Information
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