Active Ingredient: GLYCOPYRROLATE
Proprietary Name: GLYCOPYRROLATE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 1MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AA
Application Number: A040844
Product Number: 001
Approval Date: Aug 18, 2009
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status:
Prescription
Patent and Exclusivity Information