Active Ingredient: ETHINYL ESTRADIOL; LEVONORGESTREL
Proprietary Name: LEVONORGESTREL AND ETHINYL ESTRADIOL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 0.02MG;0.09MG
Reference Listed Drug: No
Reference Standard: Yes
TE Code: AB
Application Number: A079218
Product Number: 001
Approval Date: Jun 6, 2011
Applicant Holder Full Name: WATSON LABORATORIES INC
Marketing Status:
Prescription
Patent and Exclusivity Information
