Active Ingredient: PSEUDOEPHEDRINE HYDROCHLORIDE
Proprietary Name: PSEUDOEPHEDRINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 120MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A077442
Product Number: 001
Approval Date: Sep 28, 2005
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status:
Over-the-counter
Patent and Exclusivity Information