layolis fe

Generic: norethindrone, ethinyl estradiol, and ferrous fumarate

Labeler: actavis pharma, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name layolis fe
Generic Name norethindrone, ethinyl estradiol, and ferrous fumarate
Labeler actavis pharma, inc.
Dosage Form KIT
Routes
ORAL
Manufacturer
Actavis Pharma, Inc.

Identifiers & Regulatory

Product NDC 52544-064
Product ID 52544-064_82960ca4-6fe9-40c5-8688-8b3d2b65327a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA022573
Marketing Start 2011-12-23
Marketing End 2026-03-31

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 52544064
Hyphenated Format 52544-064

Supplemental Identifiers

RxCUI
1095223 1099638 1607990 1650201

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name layolis fe (source: ndc)
Generic Name norethindrone, ethinyl estradiol, and ferrous fumarate (source: ndc)
Application Number NDA022573 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 0.8 mg
  • 0.025 mg
  • 75 mg
source: label
Packaging
  • 3 BLISTER PACK in 1 CARTON (52544-064-31) / 1 KIT in 1 BLISTER PACK
source: ndc

Packages (1)

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

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Layolis Fe ndc-match (0.9)

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"}