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tekamlo

Pharmaranks rates Tekamlo 3.5/5 for recall safety — an independent score from its FDA recall history and its manufacturer's record. Tekamlo is a combination medicine containing Aliskiren Hemifumarate and Amlodipine Besylate.

Aliskiren Hemifumarate and Amlodipine Besylate · by Novartis

70/100Limited · 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 August 19, 2026·How we rate
Verified againstopenFDANIH DailyMedRxClass

Key facts

Active ingredient
Aliskiren Hemifumarate and Amlodipine Besylate
Form
Tablet
Strength
Aliskiren Hemifumarate EQ 150MG Base; Amlodipine Besylate EQ 10MG Base · Aliskiren Hemifumarate EQ 150MG Base; Amlodipine Besylate EQ 5MG Base · Aliskiren Hemifumarate EQ 300MG Base; Amlodipine Besylate EQ 10MG Base · Aliskiren Hemifumarate EQ 300MG Base; Amlodipine Besylate EQ 5MG Base
Type
Prescription (Rx)
Brand or generic
Brand-name
Manufacturer
Novartis
Half-life
about 30 to 50 hours (how long it stays in your system)
FDA application
NDA022545
Availability
Discontinued (per FDA)

How long does Aliskiren Hemifumarate and Amlodipine Besylate stay in your body?

The elimination half-life of aliskiren hemifumarate and amlodipine besylate is about 30 to 50 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 parent drug's terminal elimination half-life in adults with normal liver function; it is longer (about 56 hours) in people with impaired liver function, and elderly patients and those with liver problems or heart failure clear the drug more slowly (roughly 40 to 60% higher blood levels). Amlodipine's metabolites are inactive, so no active-metabolite caveat applies.

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: NORVASC (amlodipine besylate) tablets — FDA prescribing information, DailyMed.

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

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

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Frequently asked questions

How is Tekamlo rated?
pharmaranks gives Tekamlo a composite score of 3.5 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 Tekamlo?
pharmaranks is an independent ratings site, not a pharmacy — we don't issue coupons or sell Tekamlo. 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 Tekamlo?
Tekamlo is marketed by Novartis. You can see Novartis's full profile, rating, and other products on pharmaranks.
Is Tekamlo a brand-name or generic drug?
Tekamlo is a brand-name product with the active ingredient Aliskiren Hemifumarate and Amlodipine Besylate.
Is Tekamlo available over the counter?
No. Tekamlo 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 Tekamlo come in?
Tekamlo is currently marketed as tablet, per the FDA's National Drug Code Directory.
Is Tekamlo FDA-registered?
Tekamlo is on record with the U.S. FDA under application number NDA022545. You can verify this on its official FDA label.
Has Tekamlo been recalled by the FDA?
Tekamlo 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 Tekamlo safe?
There's no single safe-or-not verdict. pharmaranks gives Tekamlo a recall-safety score of 70/100, 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.

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