Active Ingredient: ETHINYL ESTRADIOL; NORETHINDRONE
Proprietary Name: NORETHINDRONE AND ETHINYL ESTRADIOL AND FERROUS FUMARATE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 0.035MG;0.4MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A207066
Product Number: 001
Approval Date: Mar 29, 2017
Applicant Holder Full Name: NAARI PTE LTD
Marketing Status:
Prescription
Patent and Exclusivity Information