Active Ingredient: LEVONORGESTREL
Proprietary Name: LEVONORGESTREL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 0.75MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A078665
Product Number: 001
Approval Date: Aug 28, 2009
Applicant Holder Full Name: FOUNDATION CONSUMER HEALTHCARE LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information