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norminest fe

Norminest Fe is a combination medicine containing Ethinyl Estradiol, Norethindrone, and Ferrous Fumarate.

Ethinyl Estradiol and Norethindrone and Ferrous Fumarate · by Gd Searle LLC

Not yet rated· sourced from the FDA label
Rated against independent regulatory sources·Last updated June 7, 2026·How we rate
Verified againstopenFDANIH DailyMedRxClass

Key facts

Active ingredient
Ethinyl Estradiol and Norethindrone and Ferrous Fumarate
Form
Tablet
Strength
Ethinyl Estradiol 0.035MG; Norethindrone 0.5MG; Ferrous Fumarate 75MG
Type
Prescription (Rx)
Brand or generic
Brand-name
Manufacturer
Gd Searle LLC
Half-life
about 8 hours (how long it stays in your system)
FDA application
NDA017948

How long does Ethinyl Estradiol and Norethindrone and Ferrous Fumarate stay in your body?

The elimination half-life of ethinyl estradiol and norethindrone and ferrous fumarate is about 8 hours — the time it takes the body to clear about half of it. As a rule of thumb, a medicine is mostly gone after roughly 4 to 5 half-lives, though this varies from person to person with age and kidney or liver function. This is the terminal (elimination) half-life, not a distribution phase: the label states "the mean terminal elimination half-life of norethindrone following single dose administration ... is approximately 8 hours," and its single-dose PK table gives t½ = 7.7 ± 0.5 hours (12 healthy women, 0.35 mg, fasting). Norethindrone itself is the active drug, and the label names no active metabolite that outlasts it — it is extensively reduced and then sulfate/glucuronide conjugated, with less than 5% excreted unchanged. Related point for anyone reading a different label: norethindrone ACETATE is a prodrug that is rapidly converted to norethindrone, so norethindrone is the active moiety in those products too. This label does not characterize how the half-life changes in older adults or in kidney or liver impairment — no such pharmacokinetic data is given, so no number can be quoted for those groups (the label does contraindicate use in women with significant liver disease, but that is a safety statement, not a half-life adjustment).

This is general information, not medical advice. It doesn’t tell you when a drug test would read negative (tests detect substances for different, often longer, windows) or when it’s safe to take another dose — ask your pharmacist or prescriber. Source: CAMILA (norethindrone) 0.35 mg tablets — DailyMed label, Clinical Pharmacology / Pharmacokinetics.

Dosage forms

Tablet

The forms currently marketed in the U.S., per the FDA National Drug Code Directory.

Ways to save

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Frequently asked questions

Is there a coupon or discount for Norminest Fe?
pharmaranks is an independent ratings site, not a pharmacy — we don't issue coupons or sell Norminest Fe. To pay less, ask your prescriber or pharmacist whether a generic equivalent exists, check the manufacturer's copay/savings card and patient-assistance program, and compare a pharmacy discount card against your insurance copay. Prices vary by pharmacy, insurance, and location, so always confirm at the counter. This is general reference, not medical or financial advice.
Who makes Norminest Fe?
Norminest Fe is marketed by Gd Searle LLC. You can see Gd Searle LLC's full profile, rating, and other products on pharmaranks.
Is Norminest Fe a brand-name or generic drug?
Norminest Fe is a brand-name product with the active ingredient Ethinyl Estradiol and Norethindrone and Ferrous Fumarate.
Is Norminest Fe available over the counter?
No. Norminest Fe is a prescription (Rx) medication in the US — you need a prescription from a licensed clinician (in person or via telehealth); it isn't sold over the counter. For some conditions there are OTC alternatives — ask your pharmacist.
What forms does Norminest Fe come in?
Norminest Fe is currently marketed as tablet, per the FDA's National Drug Code Directory.
Is Norminest Fe FDA-registered?
Norminest Fe is on record with the U.S. FDA under application number NDA017948. You can verify this on its official FDA label.

Information is sourced from public FDA regulatory data. Provided for general reference only — not medical advice. Always consult a licensed professional and the current prescribing information.

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