fexofenadine hydrochloride and pseudoephedrine hydrochloride
Pharmaranks rates Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride 3.4/5 for recall safety — an independent score from its FDA recall history and its manufacturer's record. Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride is a combination medicine containing Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride.
Generic · by Aurobindo Pharma Ltd
Generic of Allegra-D 12 Hour Allergy and Congestion
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 →
Key facts
- Active ingredient
- Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride
- Form
- Tablet, extended release
- Strength
- Fexofenadine Hydrochloride 180MG; Pseudoephedrine Hydrochloride 240MG
- Type
- Over-the-counter (OTC)
- Brand or generic
- Generic
- Manufacturer
- Aurobindo Pharma Ltd
- Half-life
- roughly 3 to 16 hours — the label does not give one number, because the elimination half-life depends on urine pH: about 3 to 6 hours when urine pH is 5 (acidic), and about 9 to 16 hours when urine pH is 8 (alkaline) (how long it stays in your system)
- What the pharmacy pays
- ~$7.44 for 30 — not your price
- FDA application
- ANDA215232
What is Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride?
From the FDA label:Uses temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: runny nose sneezing itchy, watery eyes itching of the nose or throat temporarily relieves nasal congestion due to the common cold, hay fever or other upper respiratory allergies reduces swelling of nasal passages temporarily relieves sinus congestion and pressure temporarily restores freer breathing through the nose
How to use
Directions do not divide, crush, chew or dissolve the tablet; swallow tablet whole adults and children 12 years of age and over take 1 tablet with a glass of water every 24 hours on an empty stomach; do not take more than 1 tablet in 24 hours children under 12 years of age do not use adults 65 years of age and older ask a doctor consumers with kidney disease ask a doctor Other information safety sealed: do not use if carton is opened or if individual blister units are torn or opened store between 20° and 25°C (68° and 77°F) FDA approved dissolution test specifications differ from USP
Warnings
Important safety information
Do not use if you have ever had an allergic reaction to this product or any of its ingredients if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson’s disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product. if you have difficulty swallowing
How long does Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride stay in your body?
The elimination half-life of fexofenadine hydrochloride and pseudoephedrine hydrochloride is roughly 3 to 16 hours — the label does not give one number, because the elimination half-life depends on urine pH: about 3 to 6 hours when urine pH is 5 (acidic), and about 9 to 16 hours when urine pH is 8 (alkaline) — 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 a genuinely variable half-life, not a fixed one. Pseudoephedrine is cleared mostly unchanged by the kidneys (55% to 96% of a dose appears unchanged in urine), and because it is a base, acidic urine traps and flushes it out faster while alkaline urine lets it be reabsorbed — hence the 3-6 h vs 9-16 h spread the label reports. No active metabolite to worry about: the label says less than 1% is metabolized in the liver, by N-demethylation, to an INACTIVE metabolite. It is not a prodrug. Kidney impairment: because clearance is renal, the label states pseudoephedrine "may accumulate in patients with renal impairment," and the product is to be generally avoided in these patients — expect a longer half-life, though the label does not quantify it. Liver impairment: no studies of pseudoephedrine were conducted in hepatic impairment, so the label gives no number; the product is likewise to be generally avoided. Older adults: this label gives no separate pseudoephedrine half-life for people 65+ (its geriatric pharmacokinetic data covers the antihistamine component only), but it warns that older adults are more likely to have adverse reactions to sympathomimetic amines. The half-life above is from the Clarinex-D 12 Hour label, which is where FDA-approved pseudoephedrine pharmacokinetics are published; standalone OTC pseudoephedrine products carry monograph "Drug Facts" labels that contain no pharmacokinetics section at all.
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: CLARINEX-D 12 HOUR (desloratadine and pseudoephedrine sulfate) extended release tablets — Section 12.3 Pharmacokinetics, DailyMed.
Dosage forms
Tablet, extended release
The forms currently marketed in the U.S., per the FDA National Drug Code Directory.
Ways to save
Ask for the generic
Same active ingredient, far cheaper. Is there a generic? →
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.
Compare alternatives
A same-class option may cost less. See alternatives →
Frequently asked questions
- How is Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride rated?
- pharmaranks gives Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride a composite score of 3.4 out of 5, currently based on 1 weighted source (FDA regulatory recall-safety data weighted highest). See our methodology at /how-we-rate.
- How much does Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride cost?
- Nobody can tell you what you will pay — your price is set by your insurer's formulary, your deductible and the pharmacy's markup, and none of those are published. What IS published is what the pharmacy paid to acquire it: about $7.44 for 30, per the CMS NADAC survey. Treat that as the floor, not the quote — ask the pharmacist for the cash price as well as your copay, because for cheap generics the cash price often wins.
- Is there a coupon or discount for Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride?
- pharmaranks is an independent ratings site, not a pharmacy — we don't issue coupons or sell Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride. To pay less, Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride 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 Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride?
- Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride is marketed by Aurobindo Pharma Ltd. You can see Aurobindo Pharma Ltd's full profile, rating, and other products on pharmaranks.
- Is Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride a brand-name or generic drug?
- Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride is a generic medication; its active ingredient is Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride. Generics contain the same active ingredient as the brand-name original and are usually lower cost.
- Is Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride available over the counter?
- Yes. Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride is an over-the-counter (OTC) product — you can buy it without a prescription. Follow the label directions and ask a pharmacist if you're unsure whether it's right for you.
- What forms does Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride come in?
- Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride is currently marketed as tablet, extended release, per the FDA's National Drug Code Directory.
- Is Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride FDA-registered?
- Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride is on record with the U.S. FDA under application number ANDA215232. You can verify this on its official FDA label.
- Has Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride been recalled by the FDA?
- Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride 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 Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride safe?
- There's no single safe-or-not verdict. pharmaranks gives Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride a recall-safety score of 68/100, 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.
Clinical content sourced from the FDA label via openFDA (U.S. FDA). View the FDA label on DailyMed → Provided for general reference only — not medical advice. Always consult a licensed professional and the current prescribing information.
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fexofenadine hydrochloride and pseudoephedrine hydrochloride
68/100