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Active Ingredient: ESMOLOL HYDROCHLORIDE
Proprietary Name: ESMOLOL HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 1GM/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A216603
Product Number: 001
Approval Date: Dec 13, 2022
Applicant Holder Full Name: AMNEAL EU LTD
Marketing Status:
Prescription
Patent and Exclusivity Information
Active Ingredient: ESMOLOL HYDROCHLORIDE
Proprietary Name: ESMOLOL HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 2GM/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A216603
Product Number: 002
Approval Date: Dec 13, 2022
Applicant Holder Full Name: AMNEAL EU LTD
Marketing Status:
Prescription
Patent and Exclusivity Information