Active Ingredient: APOMORPHINE HYDROCHLORIDE
Proprietary Name: APOMORPHINE HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; SUBCUTANEOUS
Strength: 30MG/3ML (10MG/ML)
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A212025
Product Number: 001
Approval Date: Feb 23, 2022
Applicant Holder Full Name: TRUPHARMA LLC
Marketing Status:
Prescription
Patent and Exclusivity Information
