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Molecule

Amphotericin b

Lipid-based Polyene Antifungal
Available on requestOrphanCold chainGastroenterologyAntifungals
Presentations
4
Brands
0
Manufacturers
0
Available from stock
0

Amphotericin b is a lipid-based polyene antifungal indicated for the following. It is available as liposomal injection, powder for injection and powder for injectable suspension for intravenous use. MedsAcross supplies Amphotericin b 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
Lipid-based Polyene Antifungal, Polyene Antifungal
ATC classification
A01AB04 Amphotericin b · Medications used in dentistry and periodontics, subgroup A01ABA07AA07 Amphotericin b · Diarrhoea treatments and intestinal anti-inflammatories, subgroup A07A, subgroup A07AAG01AA03 Amphotericin b · Gynaecological anti-infectives, subgroup G01A, subgroup G01AAJ02AA01 Amphotericin b · Antifungals for systemic use, subgroup J02A, subgroup J02AA
US FDA first approval
13 October 1965
EU status
Not recorded
Orphan designation
Yes
WHO essential medicine
Not recorded
India (CDSCO)
Not yet confirmed against CDSCO approval lists
Routes
Intravenous
Dosage forms
Liposomal injection, Powder for injection, Powder for injectable suspension
Identifiers
UNII 7XU7A7DROERxCUI 732CAS 1397-89-3DrugBank DB00681Q412223

Clinical information

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

Uses

Amphotericin B liposome for injection is indicated for the following: Empirical therapy for presumed fungal infection in febrile, neutropenic patients. Treatment of Cryptococcal Meningitis in HIV infected patients. Treatment of patients with Aspergillus species, Candida species and/or Cryptococcus species infections refractory to amphotericin B deoxycholate, or in patients where renal impairment or unacceptable toxicity precludes the use of amphotericin B deoxycholate. Treatment of visceral leishmaniasis. In immunocompromised patients with visceral leishmaniasis treated with amphotericin B liposome for injection, relapse rates were high following initial clearance of parasites. See DOSAGE AND ADMINISTRATION for recommended doses by indication.

Source: US FDA prescribing information

Dosing overview

Amphotericin B liposome for injection is not interchangeable or substitutable on a mg per mg basis with other amphotericin B products. Different amphotericin B products are not equivalent in terms of pharmacodynamics, pharmacokinetics and dosing. Amphotericin B liposome for injection should be administered by intravenous infusion, using a controlled infusion device, over a period of approximately 120 minutes. An in-line membrane filter may be used for the intravenous infusion of amphotericin B liposome for injection, provided THE MEAN PORE DIAMETER OF THE FILTER IS NOT LESS THAN

Source: US FDA prescribing information

Contraindications

Amphotericin B liposome for injection is contraindicated in those patients who have demonstrated or have a known hypersensitivity to amphotericin B deoxycholate or any other constituents of the product unless, in the opinion of the treating physician, the benefit of therapy outweighs the risk.

Source: US FDA prescribing information

Warnings and precautions

Anaphylaxis has been reported with amphotericin B deoxycholate and other amphotericin B-containing drugs, including amphotericin B liposome for injection. If a severe anaphylactic reaction occurs, the infusion should be immediately discontinued and the patient should not receive further infusions of amphotericin B liposome for injection.

Source: US FDA prescribing information

Side effects

The following adverse events are based on the experience of 592 adult patients (295 treated with amphotericin B liposome for injection and 297 treated with amphotericin B deoxycholate) and 95 pediatric patients (48 treated with amphotericin B liposome for injection and 47 treated with amphotericin B deoxycholate) in Study 94-0-002, a randomized double-blind, multicenter study in febrile, neutropenic patients. Amphotericin B liposome for injection and amphotericin B were infused over two hours.

Source: US FDA prescribing information

Interactions

No formal clinical studies of drug interactions have been conducted with amphotericin B liposome for injection. However, the following drugs are known to interact with amphotericin B and may interact with amphotericin B liposome for injection: Antineoplastic Agents Concurrent use of antineoplastic agents may enhance the potential for renal toxicity, bronchospasm, and hypotension. Antineoplastic agents should be given concomitantly with caution. Corticosteroids and Corticotropin (ACTH) Concurrent use of corticosteroids and ACTH may potentiate hypokalemia, which could predispose the patient to cardiac dysfunction. If used concomitantly, serum electrolytes and cardiac function should be closely monitored. Digitalis Glycosides Concurrent use may induce hypokalemia and may potentiate digitalis toxicity. When administered concomitantly, serum potassium levels should be closely monitored.

Source: US FDA prescribing information

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

All presentations

4 presentations of Amphotericin b, sorted by availability.

MedicineManufacturerRegisterAvailability
Amphotericin b 50 mg liposomal injectionIntravenousGeneric name—US FDAAvailable on request
Amphotericin b 50 mg/10 mL powder for injectionIntravenous Cold chainGeneric name—US FDAAvailable on request
Amphotericin b 50 mg/12.5 mL powder for injectable suspensionIntravenousGeneric name—US FDAAvailable on request
Amphotericin b 50 mg/12.5 mL powder for 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 13 October 1965Drugs@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 Amphotericin b in public data. This is not a list of approved uses, see the clinical information.

Questions and answers

Is Amphotericin b available for export from India?

Yes, on request. MedsAcross lists 4 presentations of Amphotericin b and sources them for licensed hospitals, importers and physicians against valid import documents.

Is Amphotericin b approved by the US FDA?

Yes. The US FDA first approved Amphotericin b on 13 October 1965, according to Drugs@FDA.

Does Amphotericin b need cold chain shipping?

At least one listed presentation of Amphotericin b must be kept cold, so it is shipped in temperature-controlled packaging. Check the storage line on each presentation.

Which ATC class is Amphotericin b in?

Amphotericin b is classified under ATC code A01AB04 (Amphotericin b).

References

  1. Amphotericin B prescribing information (Sun Pharmaceutical Industries). U.S. National Library of Medicine, DailyMed. Retrieved 20 April 2026

Request Amphotericin b for export supply

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