Active Ingredient: ALBUTEROL SULFATE
Proprietary Name: ALBUTEROL SULFATE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 2MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: BX
Application Number: A210948
Product Number: 001
Approval Date: Mar 15, 2019
Applicant Holder Full Name: AIZANT DRUG RESEARCH SOLUTIONS PRIVATE LTD
Marketing Status:
Prescription
Patent and Exclusivity Information