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Active Ingredient: ATROPINE SULFATE
Proprietary Name: ATROPINE SULFATE
Dosage Form; Route of Administration: SOLUTION; INTRAVENOUS
Strength: 0.5MG/5ML (0.1MG/ML)
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A215342
Product Number: 001
Approval Date: Jan 26, 2022
Applicant Holder Full Name: AMNEAL EU LTD
Marketing Status:
Prescription
Patent and Exclusivity Information
Active Ingredient: ATROPINE SULFATE
Proprietary Name: ATROPINE SULFATE
Dosage Form; Route of Administration: SOLUTION; INTRAVENOUS
Strength: 1MG/10ML (0.1MG/ML)
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A215342
Product Number: 002
Approval Date: Oct 25, 2023
Applicant Holder Full Name: AMNEAL EU LTD
Marketing Status:
Prescription
Patent and Exclusivity Information