Larin 1.5/30
LARIN™ 1.5/30（Norethindrone Acetate and Ethinyl Estradiol Tablets, USP）
Approved
Approval ID
e232ed29-e6f5-4591-8d61-68eb8b1596f0
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Oct 26, 2023
Manufacturers
FDA
Northstar Rx LLC
DUNS: 830546433
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Norethindrone Acetate/Ethinyl Estradiol
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code16714-407
Application NumberANDA202996
Product Classification
M
Marketing Category
C73584
G
Generic Name
Norethindrone Acetate/Ethinyl Estradiol
Product Specifications
Effective DateDecember 5, 2017
FDA Product Classification