Levonorgestrel and Ethinyl Estradiol
Levonorgestrel and Ethinyl Estradiol Tablets USP 0.15mg/0.03 mg
Approved
Approval ID
ea9f7216-0358-43a9-96eb-5dad694ae9b8
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Apr 5, 2023
Manufacturers
FDA
Naari Pte Limited
DUNS: 659345996
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Levonorgestrel and Ethinyl Estradiol
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code79929-003
Application NumberANDA207033
Product Classification
M
Marketing Category
C73584
G
Generic Name
Levonorgestrel and Ethinyl Estradiol
Product Specifications
Effective DateApril 5, 2023
FDA Product Classification