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Molecule

Aminophylline

Also known as aminophylline dihydrate
Available on requestRespiratory
Presentations
3
Brands
0
Manufacturers
0
Available from stock
0

Aminophylline is a methylxanthine. It is available as injection for intravenous use. MedsAcross supplies Aminophylline for export from India to licensed hospitals, importers and physicians acting for named patients, with the documents each country requires.

Information from the US FDA prescribing information, retrieved 12 November 2026. Not yet medically reviewed.How we review

Key facts

Pharmacological class
Methylxanthine
ATC classification
R03DA05 Aminophylline · Xanthines
US FDA first approval
19 April 1940
EU status
Not recorded
Orphan designation
Not recorded
WHO essential medicine
Not recorded
India (CDSCO)
Not yet confirmed against CDSCO approval lists
Routes
Intravenous
Dosage forms
Injection
Identifiers
UNII 27Y3KJK423RxCUI 689CAS 317-34-0DrugBank DB01223Q471763

Clinical information

From the regulator-approved product information. Each section names its source.

Uses

Intravenous theophylline is indicated as an adjunct to inhaled beta-2 selective agonists and systemically administered corticosteroids for the treatment of acute exacerbations of the symptoms and reversible airflow obstruction associated with asthma and other chronic lung diseases, e.g., emphysema and chronic bronchitis.

Source: US FDA prescribing information

How it works

Theophylline has two distinct actions in the airways of patients with reversible obstruction, smooth muscle relaxation (i.e., bronchodilation) and suppression of the response of the airways to stimuli (i.e., nonbronchodilator prophylactic effects). While the mechanisms of action of theophylline are not known with certainty, studies in animals suggest that bronchodilation is mediated by the inhibition of two isozymes of phosphodiesterase (PDE III and, to a lesser extent, PDE IV), while nonbronchodilator prophylactic actions are probably mediated through one or more different molecular mechanisms, that do not involve inhibition of PDE III or antagonism of adenosine receptors.

Source: US FDA prescribing information

Dosing overview

General Considerations: The steady-state serum theophylline concentration is a function of the infusion rate and the rate of theophylline clearance in the individual patient. Because of marked individual differences in the rate of theophylline clearance, the dose required to achieve a serum theophylline concentration in the 10-20 mcg/mL range varies fourfold among otherwise similar patients in the absence of factors known to alter theophylline clearance. For a given population there is no single theophylline dose that will provide both safe and effective serum concentrations for all patients. Administration of the median theophylline dose required to achieve a therapeutic serum theophylline concentration in a given population may result in either sub-therapeutic or potentially toxic serum theophylline concentrations in individual patients.

Source: US FDA prescribing information

Contraindications

Aminophylline is contraindicated in patients with a history of hypersensitivity to theophylline or other components in the product including ethylenediamine.

Source: US FDA prescribing information

Warnings and precautions

Concurrent Illness: Theophylline should be used with extreme caution in patients with the following clinical conditions due to the increased risk of exacerbation of the concurrent condition: Active peptic ulcer disease Seizure disorders Cardiac arrhythmias (not including bradyarrhythmias) Conditions That Reduce Theophylline Clearance: There are several readily identifiable causes of reduced theophylline clearance. If the infusion rate is not appropriately reduced in the presence of these risk factors, severe and potentially fatal theophylline toxicity can occur.

Source: US FDA prescribing information

Side effects

Adverse reactions associated with theophylline are generally mild when peak serum theophylline concentrations are <20 mcg/mL and mainly consist of transient caffeine-like adverse effects such as nausea, vomiting, headache, and insomnia. When peak serum theophylline concentrations exceed 20 mcg/mL, however, theophylline produces a wide range of adverse reactions including persistent vomiting, cardiac arrhythmias, and intractable seizures which can be lethal. Other adverse reactions that have been reported at serum theophylline concentrations <20 mcg/mL include diarrhea, irritability, restlessness, fine skeletal muscle tremors, and transient diuresis.

Source: US FDA prescribing information

Interactions

Theophylline interacts with a wide variety of drugs. The interaction may be pharmacodynamic, i.e., alterations in the therapeutic response to theophylline or another drug or occurrence of adverse effects without a change in serum theophylline concentration. More frequently, however, the interaction is pharmacokinetic, i.e., the rate of theophylline clearance is altered by another drug resulting in increased or decreased serum theophylline concentrations. Theophylline only rarely alters the pharmacokinetics of other drugs. The drugs listed in Table II have the potential to produce clinically significant pharmacodynamic or pharmacokinetic interactions with theophylline. The information in the "Effect" column of Table II assumes that the interacting drug is being added to a steady-state theophylline regimen.

Source: US FDA prescribing information

For healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.

All presentations

3 presentations of Aminophylline, sorted by availability.

MedicineManufacturerRegisterAvailability
Aminophylline 500 mg/20 mL injectionIntravenousGeneric name—US FDAAvailable on request
Aminophylline 250 mg/10 mL injectionIntravenousGeneric name—US FDAAvailable on request
Aminophylline 25 mg/1 mL injectionIntravenousGeneric name—US FDAAvailable on request

Regulatory status

Approval facts from US FDA, EMA and CDSCO data, and registration status by country where we hold register data.

RegisterStatusSource
US FDAFirst approved 19 April 1940Drugs@FDA
EU (EMA)Not recorded—
India (CDSCO)Not yet confirmed against CDSCO approval lists—
United StatesRegisteredUS FDA (NDC directory, openFDA)Checked 12 November 2026

Conditions

Conditions linked to Aminophylline in public data. This is not a list of approved uses, see the clinical information.

Questions and answers

Is Aminophylline available for export from India?

Yes, on request. MedsAcross lists 3 presentations of Aminophylline and sources them for licensed hospitals, importers and physicians against valid import documents.

Is Aminophylline approved by the US FDA?

Yes. The US FDA first approved Aminophylline on 19 April 1940, according to Drugs@FDA.

Does Aminophylline need cold chain shipping?

No listed presentation of Aminophylline is recorded as needing a cold chain. Storage conditions are shown on each presentation page.

Which ATC class is Aminophylline in?

Aminophylline is classified under ATC code R03DA05 (Aminophylline).

References

  1. Aminophylline prescribing information (Hospira). U.S. National Library of Medicine, DailyMed. Retrieved 22 May 2026

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