Reliable Hypertension Treatment
The first and only patent-pending, FDA-approved, amlodipine powder formulation. Ideal for pediatric, geriatric, and dysphagic patients requiring ease-of-use and precision, as well as tube-fed patients.
Learn MoreRx Available by prescription only
Prescription Strength Powdered Oral Solution
Sdamlo™ provides reliable and consistent hypertension treatment while ensuring accurate and easy administration via single-dose bottles. Perfect for pediatric, geriatric, and dysphagic patients. Available by prescription-only.
Easy-to-Swallow
Powdered oral solution that offers flexible, easy-to-swallow, dosing that supports accurate administration for patients who have difficulty with solid dosage forms.
Easy-to-Take
Convenient unit-dose containers allow for easy and precise delivery of medication, ensuring patients receive the exact amount prescribed. No measuring, shaking, or stirring required.
Alcohol-Free
Alcohol is a common excipient in many amlodipine liquid formulations, which can reduce their appropriateness for pediatric and geriatric populations. Sdamlo™ is alcohol-free.
Preservative-Free
To reach the widest patient pool and benefit the most patients, in addition to being alcohol-free, Sdamlo™ is also preservative-free and Sucralose-free.
Treatment Centered Around You
Sdamlo™ provides a superior liquid dosage form that is easier to administer than other liquid and solid amlodipine oral medications. Our powder for oral solution supports treatment adherence in dysphagic, geriatric and pediatric patients, as well as tube-fed patients and patients undergoing immunotherapy.
Easy-to-Swallow
Our powder oral solution format eliminates the need to swallow tablets, reducing aspiration risk and promoting patient's daily use, aiding patients with oropharyngeal dysphagia, pharyngeal dysphagia, and esophageal dysphagia.
Alcohol-Free
Sdamlo™ avoids the use of alcohol commonly found in liquid formulations, enhancing suitability for dysphagic, pediatric, and geriatric populations. Additionally, Sdamlo™ is preservative-free and sucralose-free.
"No Guess" Dosing
Our convenient unit-dose containers allow for easy and precise delivery of medication, ensuring patients receive the exact amount prescribed. Simplified unit-dose treatment improves patient and care giver confidence, promoting more optimal outcomes.
No Refrigeration Required
No refrigeration, measuring, shaking, or stirring of Sdamlo™ is required. Simply open, add water, and take the medication. See our medication guide for full instructions.
Accurate Dosing Every Time
Our convenient unit-dose containers allow for easy and precise delivery of medication, ensuring patients receive the exact amount prescribed. No measuring, shaking, or stirring required. Patient-centered, simplified unit-dose treatment improves patient and care giver confidence, promoting more optimal outcomes.
Eliminate the Risk Associated with Compounding
Patients who have difficulty swallowing are often given crushed/compounded formulations of the prescriptions. However, crushed/compounded formulations can exhibit a wide variation in potency due to non-uniformity of compounded materials. Sdamlo™ is consistent and easy-to-use, helping you avoid the risks associated with compounded medications.
In 2007, the CDC found compounded drugs have a higher risk of contamination. Sdamlo™ eliminates this compounding variability and dosing risk.
Crushed and compounded products can have variable and very costly, short shelf lives, while our manufacturer-controlled formulation offers consistent accuracy and integrity.
Pay as little as $0* for your medication
No patient registration is required to use our copay voucher and the savings can be applied to initial prescriptions, refills, and 30 or 90-day prescription supply. Savings available only to eligible commercially insured patients.
Simply present to your pharmacist
* When the maximum savings benefit is not exceeded for eligible patients
Further Resources
Browse our resources below for further specifics and information on Sdamlo™
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Instructional Video
Source: Sdamlo™
Watch our instructional video on how to take or give Sdamlo™.
View Instructional Video -
How to Administer Sdamlo™
Source: Sdamlo™
Consult the following Sdamlo™ Administration Guide before taking or giving Sdamlo™.
View/Download -
Risks of Pharmacy Compounding
Source: National Institutes of Health
Regulatory oversight of pharmacy compounding is significantly less rigorous than that required for Food and Drug Administration (FDA)-approved drugs; as such, compounded drugs may pose additional risks to patients.
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Additional Medical Information; Rx only
Indications & Usage
Sdamlo™ is a calcium channel blocker and may be used alone or in combination with other antihypertensive and antianginal agents for the treatment of:
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Hypertension
Sdamlo™ is indicated for the treatment of hypertension, to lower blood pressure in adults and pediatric patients 6 years of age and older. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions.
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Coronary Artery Disease in adults
Chronic Stable Angina
Vasospastic Angina (Prinzmetal's or Variant Angina)
Angiographically Documented Coronary Artery Disease in patients without heart failure or an ejection fraction <40%
Please see Full Prescribing Information, including Boxed Warning, and Important Safety Information on the product itself and/or on www.sdamlorx.com.
Individual patient results may vary. To report suspected adverse reactions, contact the FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. You may also contact Pangea Pharmaceuticals at 855-892-8224 or drugsafety@pangeapharm.com.
How Supplied
Sdamlo™ are supplied as unit-dose powder for oral administration. Sdamlo™ contains 2.5 mg, 5 mg, or 10 mg of amlodipine, USP. NDCs 81279-133-10, 81279-134-10, and 81279-135-10 respectively.
Contraindications
Sdamlo™ are contraindicated in patients with a known sensitivity to amlodipine.
Warnings & Precautions
Symptomatic hypotension is possible, particularly in patients with severe aortic stenosis. However, acute hypotension is unlikely.
Worsening angina and acute myocardial infarction can develop after starting or increasing the dose of Sdamlo™, particularly in patients with severe obstructive coronary artery disease.
Titrate slowly in patients with severe hepatic impairment.
Adverse Reactions
Most common adverse reaction to amlodipine is edema which occurred in a dose related manner. Other adverse experiences not dose related but reported with an incidence >1.0% are fatigue, nausea, abdominal pain, and somnolence.
For complete prescribing and dosage information click here