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quasense

Pharmaranks rates Quasense 3.6/5 for recall safety — an independent score from its FDA recall history and its manufacturer's record. Quasense is a combination medicine containing Ethinyl Estradiol and Levonorgestrel.

Ethinyl Estradiol and Levonorgestrel · by Watson Labs

Generic of Loseasonique

72/100Limited · 1 source

Based on 1 source · Recall-safety score from FDA recall history — this product's own recalls and its manufacturer's record. Not an efficacy or quality rating. methodology →

Rated against independent regulatory sources·Last updated October 10, 2026·How we rate
Verified againstopenFDANIH DailyMedRxClass

Key facts

Active ingredient
Ethinyl Estradiol and Levonorgestrel
Form
Tablet
Strength
Ethinyl Estradiol 0.03MG; Levonorgestrel 0.15MG
Type
Prescription (Rx)
Brand or generic
Generic
Manufacturer
Watson Labs
Half-life
about 36 hours (36 ± 13 hours at steady state) (how long it stays in your system)
FDA application
ANDA077101

How long does Ethinyl Estradiol and Levonorgestrel stay in your body?

The elimination half-life of ethinyl estradiol and levonorgestrel is about 36 hours (36 ± 13 hours at steady state) — 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 stated directly for levonorgestrel; the label reports no active metabolite that outlasts the parent, and levonorgestrel is not a prodrug. The number comes from a levonorgestrel/ethinyl estradiol combination oral-contraceptive label (Aviane), where it is attributed specifically to the levonorgestrel component; the single-ingredient OTC emergency-contraceptive labels do not state a half-life. On populations: the label says no formal studies evaluated hepatic or renal impairment, but cautions that steroid hormones may be poorly metabolized in patients with impaired liver function; it notes no apparent pharmacokinetic differences across races, and states nothing about older adults.

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: Aviane (levonorgestrel and ethinyl estradiol) label — DailyMed, Clinical Pharmacology / Pharmacokinetics.

Dosage forms

Tablet

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

Ways to save

Ask for the generic

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Request a 90-day supply

Bulk fills usually lower the per-dose price vs monthly refills.

Use copay cards

Manufacturer copay cards & patient-assistance programs — especially for brand drugs.

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Frequently asked questions

How is Quasense rated?
pharmaranks gives Quasense a composite score of 3.6 out of 5, currently based on 1 weighted source (FDA regulatory recall-safety data weighted highest). See our methodology at /how-we-rate.
Is there a coupon or discount for Quasense?
pharmaranks is an independent ratings site, not a pharmacy — we don't issue coupons or sell Quasense. To pay less, Quasense is already a generic — usually the lowest-cost version — so the main levers are comparing cash prices between pharmacies and using a pharmacy discount-card service. Prices vary by pharmacy, insurance, and location, so always confirm at the counter. This is general reference, not medical or financial advice.
Who makes Quasense?
Quasense is marketed by Watson Labs. You can see Watson Labs's full profile, rating, and other products on pharmaranks.
Is Quasense a brand-name or generic drug?
Quasense is a generic medication; its active ingredient is Ethinyl Estradiol and Levonorgestrel. Generics contain the same active ingredient as the brand-name original and are usually lower cost.
Is Quasense available over the counter?
No. Quasense 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 Quasense come in?
Quasense is currently marketed as tablet, per the FDA's National Drug Code Directory.
Is Quasense FDA-registered?
Quasense is on record with the U.S. FDA under application number ANDA077101. You can verify this on its official FDA label.
Has Quasense been recalled by the FDA?
Quasense has no FDA recalls recorded under its own application in the openFDA enforcement database. Its recall-safety score reflects its manufacturer's overall recall record. This is general reference, not medical advice — check the FDA recall database for the latest alerts.
Is Quasense safe?
There's no single safe-or-not verdict. pharmaranks gives Quasense a recall-safety score of 72/100, based on its FDA recall history (no recalls under its own FDA application) — not an efficacy or side-effect rating. Review its FDA-label side effects and warnings before use, and always consult a licensed professional.

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.

What people report to the FDA about ETHINYL ESTRADIOL AND LEVONORGESTREL

The FDA Adverse Event Reporting System (FAERS) collects reports from patients and clinicians. It holds 91 reports naming ETHINYL ESTRADIOL AND LEVONORGESTREL — the active ingredient in Quasense, and the FDA flagged 92% of those reports as serious. The effects reported most often — leaving out reports about overdose, misuse or the condition being treated, which dominate the raw list for common medicines:

  • drug exposure during pregnancy9 reports
  • nausea8 reports
  • vomiting8 reports
  • pregnancy on oral contraceptive7 reports
  • abdominal pain6 reports
  • pruritus6 reports
  • cytolytic hepatitis5 reports
  • asthenia4 reports

Read these as a signal, not a rate. A report does not mean ETHINYL ESTRADIOL AND LEVONORGESTREL caused the effect — anyone can file one, and many describe people taking several medicines for several conditions. Crucially there is no denominator: FAERS does not record how many people took the drug, so these counts cannot be turned into “X% of patients” — a bigger number often just means a more widely used or more talked-about drug. Duplicates exist, and publicity drives reporting. For what is actually established, read the FDA label.

Source: openFDA drug/event (FAERS), retrieved September 25, 2026.

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quasense

72/100