Active Ingredient: LEVALBUTEROL HYDROCHLORIDE
Proprietary Name: LEVALBUTEROL HYDROCHLORIDE
Dosage Form; Route of Administration: SOLUTION; INHALATION
Strength: EQ 0.25% BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: AN
Application Number: A207628
Product Number: 001
Approval Date: Jan 31, 2017
Applicant Holder Full Name: LUOXIN AUROVITAS PHARMA CHENGDU CO LTD
Marketing Status:
Prescription
Patent and Exclusivity Information
