Package 52544-064-31

Brand: layolis fe

Generic: norethindrone, ethinyl estradiol, and ferrous fumarate
NDC Package

Package Facts

Identity

Package NDC 52544-064-31
Digits Only 5254406431
Product NDC 52544-064
Product ID 52544-064_82960ca4-6fe9-40c5-8688-8b3d2b65327a
Description

3 BLISTER PACK in 1 CARTON (52544-064-31) / 1 KIT in 1 BLISTER PACK

Marketing

Marketing Status
Discontinued 2026-03-31
Brand layolis fe
Generic norethindrone, ethinyl estradiol, and ferrous fumarate
Sample Package No

Linked Drug Pages (1)

Layolis Fe ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "82960ca4-6fe9-40c5-8688-8b3d2b65327a", "openfda": {"rxcui": ["1095223", "1099638", "1607990", "1650201"], "spl_set_id": ["c0db84ca-b8d4-4ed2-b2f6-19347283146e"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (52544-064-31)  / 1 KIT in 1 BLISTER PACK", "package_ndc": "52544-064-31", "marketing_end_date": "20260331", "marketing_start_date": "20111223"}], "brand_name": "Layolis Fe", "product_id": "52544-064_82960ca4-6fe9-40c5-8688-8b3d2b65327a", "dosage_form": "KIT", "product_ndc": "52544-064", "generic_name": "norethindrone, ethinyl estradiol, and ferrous fumarate", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Layolis Fe", "application_number": "NDA022573", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_end_date": "20260331", "marketing_start_date": "20111223"}