lo loestrin fe
Generic: norethindrone acetate and ethinyl estradiol, ethinyl estradiol and ferrous fumarate
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
lo loestrin fe
Generic Name
norethindrone acetate and ethinyl estradiol, ethinyl estradiol and ferrous fumarate
Labeler
a-s medication solutions
Dosage Form
KIT
Manufacturer
Identifiers & Regulatory
Product NDC
50090-1456
Product ID
50090-1456_df0357bd-d2b1-4593-adcc-d8eef3e22260
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
500901456
Hyphenated Format
50090-1456
Supplemental Identifiers
RxCUI
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
Packaging
- 1 KIT in 1 KIT (50090-1456-0)
Packages (1)
Ingredients (0)
No ingredient records.
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"spl_id": "df0357bd-d2b1-4593-adcc-d8eef3e22260", "openfda": {"rxcui": ["248310", "259176", "1037183", "1037184", "1037185"], "spl_set_id": ["e2f24e91-4893-40bf-b310-d93db95d2442"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 KIT (50090-1456-0)", "package_ndc": "50090-1456-0", "marketing_start_date": "20141128"}], "brand_name": "LO LOESTRIN FE", "product_id": "50090-1456_df0357bd-d2b1-4593-adcc-d8eef3e22260", "dosage_form": "KIT", "product_ndc": "50090-1456", "generic_name": "norethindrone acetate and ethinyl estradiol, ethinyl estradiol and ferrous fumarate", "labeler_name": "A-S Medication Solutions", "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"}