lo loestrin fe

Generic: norethindrone acetate and ethinyl estradiol, ethinyl estradiol and ferrous fumarate

Labeler: allergan, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name lo loestrin fe
Generic Name norethindrone acetate and ethinyl estradiol, ethinyl estradiol and ferrous fumarate
Labeler allergan, inc.
Dosage Form KIT
Manufacturer
Allergan, Inc.

Identifiers & Regulatory

Product NDC 0430-0420
Product ID 0430-0420_4b7cbcd3-7192-43cf-bd16-98bc8ed95645
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA022501
Listing Expiration 2026-12-31
Marketing Start 2010-12-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 04300420
Hyphenated Format 0430-0420

Supplemental Identifiers

RxCUI
248310 259176 1037183 1037184 1037185

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 lo loestrin fe (source: ndc)
Generic Name norethindrone acetate and ethinyl estradiol, ethinyl estradiol and ferrous fumarate (source: ndc)
Application Number NDA022501 (source: ndc)

Resolved Composition

Strengths
  • 1 mg
  • 10 mcg
  • 75 mg
source: label
Packaging
  • 5 BLISTER PACK in 1 CARTON (0430-0420-14) / 1 KIT in 1 BLISTER PACK
  • 8 CARTON in 1 TRAY (0430-0420-60) / 30 BLISTER PACK in 1 CARTON / 1 KIT in 1 BLISTER PACK
  • 6 CARTON in 1 TRAY (0430-0420-95) / 1 BLISTER PACK in 1 CARTON / 1 KIT in 1 BLISTER PACK
source: ndc

Packages (3)

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"spl_id": "4b7cbcd3-7192-43cf-bd16-98bc8ed95645", "openfda": {"rxcui": ["248310", "259176", "1037183", "1037184", "1037185"], "spl_set_id": ["c33072cf-625d-4b4a-981e-ec049c5d78aa"], "manufacturer_name": ["Allergan, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 BLISTER PACK in 1 CARTON (0430-0420-14)  / 1 KIT in 1 BLISTER PACK", "package_ndc": "0430-0420-14", "marketing_start_date": "20101201"}, {"sample": false, "description": "8 CARTON in 1 TRAY (0430-0420-60)  / 30 BLISTER PACK in 1 CARTON / 1 KIT in 1 BLISTER PACK", "package_ndc": "0430-0420-60", "marketing_start_date": "20101201"}, {"sample": false, "description": "6 CARTON in 1 TRAY (0430-0420-95)  / 1 BLISTER PACK in 1 CARTON / 1 KIT in 1 BLISTER PACK", "package_ndc": "0430-0420-95", "marketing_start_date": "20101201"}], "brand_name": "Lo Loestrin Fe", "product_id": "0430-0420_4b7cbcd3-7192-43cf-bd16-98bc8ed95645", "dosage_form": "KIT", "product_ndc": "0430-0420", "generic_name": "norethindrone acetate and ethinyl estradiol, ethinyl estradiol and ferrous fumarate", "labeler_name": "Allergan, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lo Loestrin Fe", "application_number": "NDA022501", "marketing_category": "NDA", "marketing_start_date": "20101201", "listing_expiration_date": "20261231"}