Active Ingredient: DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM
Proprietary Name: NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 25MG;220MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A213663
Product Number: 001
Approval Date: Sep 24, 2020
Applicant Holder Full Name: GRANULES INDIA LTD
Marketing Status:
Over-the-counter
Patent and Exclusivity Information