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Molecule

Atropine

Also known as atropine sulfate
Available on requestOphthalmologyGastroenterology
Presentations
19
Brands
2
Manufacturers
2
Available from stock
0

Atropine is an anticholinergic indicated for the treatment of poisoning by susceptible organophosphorus nerve agents having cholinesterase activity as well as organophosphorus or carbamate insecticides in adult and pediatric patients. MedsAcross supplies Atropine 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
Anticholinergic, Cholinergic Muscarinic Antagonist, Cholinergic Antagonists, Cholinergic Muscarinic Antagonists
ATC classification
A03BA01 Atropine · Medicines for gut spasm and motility, subgroup A03B, subgroup A03BAS01FA01 Atropine · Eye medicines, subgroup S01F, subgroup S01FA
US FDA first approval
15 May 1973
EU status
Authorised
Orphan designation
No
WHO essential medicine
Not recorded
India (CDSCO)
Not yet confirmed against CDSCO approval lists
Routes
Intravenous, Ophthalmic, Intramuscular, Endotracheal, Subcutaneous, Intramedullary, Intravascular
Dosage forms
Injection, Eye drops, Ophthalmic solution
Identifiers
UNII 7C0697DR9IRxCUI 1223DrugBank DB00572Q26272

Clinical information

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

Uses

ATROPEN is indicated for the treatment of poisoning by susceptible organophosphorus nerve agents having cholinesterase activity as well as organophosphorus or carbamate insecticides in adult and pediatric patients. ATROPEN is a cholinergic muscarinic antagonist indicated for the treatment of poisoning by susceptible organophosphorus nerve agents having cholinesterase activity as well as organophosphorus or carbamate insecticides in adult and pediatric patients.

Source: US FDA prescribing information

How it works

Atropine competitively blocks the effects of acetylcholine, including excess acetylcholine due to organophosphorus poisoning, at muscarinic cholinergic receptors on smooth muscle, cardiac muscle, secretory gland cells, and in peripheral autonomic ganglia and the central nervous system.

Source: US FDA prescribing information

Dosing overview

ATROPEN is a single-dose autoinjector intended as an initial treatment of the muscarinic symptoms of insecticide or nerve agent poisonings, definitive medical care should be sought immediately. Dosage is dependent on weight. Dosage for Mild Symptoms: If the patient experiences two or more mild symptoms, administer one injection intramuscularly into the mid-lateral thigh. If, at any time after the first dose, the patient develops any of the severe symptoms, administer two additional injections intramuscularly in rapid succession. Dosage for Severe Symptoms: If the patient is either unconscious or has any of the severe symptoms, immediately administer three injections intramuscularly into the patient's mid-lateral thigh in rapid succession.

Source: US FDA prescribing information

Warnings and precautions

Cardiovascular (CV) Risks: Tachycardia, palpitations, premature ventricular contractions, flutter, fibrillation, etc. Use caution in patients with known CV disease or conduction problems. Heat Injury: May inhibit sweating and lead to hyperthermia, avoid excessive exercising and heat exposure. Acute Glaucoma: May precipitate in susceptible individuals. Urinary Retention: May precipitate in patient with bladder outflow obstruction. Pyloric Stenosis: May precipitate complete obstruction. Exacerbation of Chronic Lung Disease: Atropine may cause inspissation of bronchial secretions and formation of dangerous viscid plugs in individuals with chronic lung disease, monitor respiratory status. Hypersensitivity: Atropine may cause hypersensitivity reactions, including anaphylaxis.

Source: US FDA prescribing information

Side effects

The following serious adverse reactions are described elsewhere in the labeling: Cardiovascular Risks Heat Injury Acute Glaucoma Urinary Retention Pyloric Stenosis Exacerbation of Chronic Lung Disease Hypersensitivity The following adverse reactions associated with the use of atropine were identified in the literature. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure. Mild to moderate pain may be experienced at the site of injection. Common adverse reactions of atropine include dryness of mouth, blurred vision, dry eyes, photophobia, confusion, headache, dizziness, tachycardia, palpitations, flushing, urinary hesitance or retention, constipation, abdominal pain, abdominal distention, nausea, vomiting, loss of libido, and impotency.

Source: US FDA prescribing information

Interactions

Pralidoxime: The signs of atropinization (flushing, mydriasis, tachycardia, dryness of the mouth and nose) may occur earlier than might be expected than when atropine is used alone. Barbiturates: Atropine may potentiate the effect of barbiturates.

Source: US FDA prescribing information

Storage

Store between 20ºC to 25ºC (68ºF to 77ºF), excursions permitted between 15ºC and 30ºC (between 59ºF and 86ºF). Keep from freezing. Protect from light.

Source: US FDA prescribing information

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

All presentations

19 presentations of Atropine, sorted by availability.

MedicineManufacturerRegisterAvailability
Atropine 10 mg/mL eye dropsOphthalmicGeneric name—US FDAAvailable on request
Atropine 1 mg/10 mL injectionIntravenousGeneric name—US FDAAvailable on request
Atropine 8 mg/20 mL injectionEndotracheal, intramedullary, intramuscular, intravenous, subcutaneousGeneric name—US FDAAvailable on request
Atropine 0.4 mg/1 mL injectionIntravenousGeneric name—US FDAAvailable on request
Atropine 1 mg/1 mL injectionIntravenousGeneric name—US FDAAvailable on request
Atropine 0.5 mg/5 mL injectionIntravenousGeneric name—US FDAAvailable on request
Atropine 10 mg/mL ophthalmic solutionOphthalmicGeneric name—US FDAAvailable on request
Atropine 0.25 mg/5 mL injectionIntravenousGeneric name—US FDAAvailable on request
Atropine 1 mg/10 mL injectionEndotracheal, intramuscular, intravenous, subcutaneousGeneric name—US FDAAvailable on request
ATROPEN Auto-Injector 2 mg/0.7 mL injectionIntramuscularMeridian Medical TechnologiesUS FDAAvailable on request
ATROPEN Auto-Injector 0.25 mg/0.3 mL injectionIntramuscularMeridian Medical TechnologiesUS FDAAvailable on request
ATROPEN Auto-Injector 0.5 mg/0.7 mL injectionIntramuscularMeridian Medical TechnologiesUS FDAAvailable on request
ATROPEN Auto-Injector 1 mg/0.7 mL injectionIntramuscularMeridian Medical TechnologiesUS FDAAvailable on request
Atropine 0.1 mg/mL injectionIntravenousGeneric name—US FDAAvailable on request
Atropine 0.25 mg/5 mL injectionEndotracheal, intramuscular, intravenous, subcutaneousGeneric name—US FDAAvailable on request
Atropine 0.4 mg/1 mL injectionIntravascularGeneric name—US FDAAvailable on request
Atropine 2 mg/0.7 mL injectionIntramuscularGeneric name—US FDAAvailable on request
Atropine 0.4 mg/mL injectionIntravenousGeneric name—US FDAAvailable on request
Isopto Atropine 10 mg/mL ophthalmic solutionOphthalmicAlcon LaboratoriesUS FDAAvailable on request

Brands by market

2 brand names across 1 markets.

Brand names by country

Manufacturers

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 15 May 1973Drugs@FDA
EU (EMA)AuthorisedEMA medicines data
India (CDSCO)Not yet confirmed against CDSCO approval lists—
AustriaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
BelgiumRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
BulgariaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
CroatiaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
CyprusRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
CzechiaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
DenmarkRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
EstoniaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
FinlandRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
FranceRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
GermanyRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
GreeceRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
HungaryRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
IcelandRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
IrelandRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
ItalyRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LatviaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LiechtensteinRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LithuaniaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LuxembourgRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
MaltaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
NetherlandsRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
NorwayRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
PolandRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
PortugalRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
RomaniaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SlovakiaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SloveniaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SpainRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SwedenRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
United StatesRegisteredUS FDA (NDC directory, openFDA)Checked 12 November 2026

Conditions

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

Questions and answers

Is Atropine available for export from India?

Yes, on request. MedsAcross lists 19 presentations of Atropine and sources them for licensed hospitals, importers and physicians against valid import documents.

What brand names does Atropine have?

The catalogue lists 2 brand names for Atropine, including ATROPEN Auto-Injector, Isopto Atropine.

Is Atropine approved by the US FDA?

Yes. The US FDA first approved Atropine on 15 May 1973, according to Drugs@FDA.

Is Atropine authorised in the European Union?

Yes. Atropine has a central EU marketing authorisation (status: authorised), according to European Medicines Agency data.

Does Atropine need cold chain shipping?

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

Which ATC class is Atropine in?

Atropine is classified under ATC code A03BA01 (Atropine).

References

  1. ATROPEN Auto-Injector prescribing information (Meridian Medical Technologies). U.S. National Library of Medicine, DailyMed. Retrieved 15 September 2022
  2. Ryjunea: European public assessment report (EPAR). European Medicines Agency. Retrieved 22 July 2026

Request Atropine for export supply

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