Skip to content
MedsAcross

Medicine

Famotidine 40 mg/5 mL powder for oral suspension

Famotidine · Oral
Available on requestPrescription onlyUS FDAGeneric name

Famotidine 40 mg/5 mL powder for oral suspension is a generic prescription medicine for oral use, made by 21 labelers, with its source record on the US FDA register. It is available on request for export supply from India to licensed hospitals, importers and physicians.

Availability

Available on request

Export supply from India to licensed buyers

Typical lead time

On request

Counted from payment and complete documents

Shipping

Ambient

Protect from freezing. Store famotidine for oral suspension dry powder and…

Key facts

Active ingredient (INN)
Famotidine
Brand
Sold under the generic name
Strength
40 mg/5 mL
Dosage form
Powder for oral suspension
Route
Oral
Packs
50 mL, 55 mL, 100 mL and 23 more
Manufacturers
LupinIndiaAjanta PharmaIndiaAscend LaboratoriesIndiaAurobindo PharmaIndiaBioconIndiaCamber PharmaceuticalsIndiaDr. Reddy's LaboratoriesIndiaMicro LabsIndiaNovadoz PharmaceuticalsIndiaZydus LifesciencesIndia
Origin register
US FDA, United States
Storage
Protect from freezing. Store famotidine for oral suspension dry powder and constituted suspension at 25°C (77°F), excursions permitted to 15° to 30°C (59° to 86°F).
Cold chain
Not required on record
Prescription status
Prescription only
Controlled substance
Not recorded as controlled
ATC code
A02BA03 Famotidine
HS code (indicative)
3004.90Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
29 June 2010
Identifiers
RxCUI 310274DailyMed set ID 45df5fae-b28a-4b48-95ef-96e4faad883f, a88e7069-230c-4105-ade0-a98968e18671, c013654e-9cad-4c59-8fea-b00ae1567c18 +21NDC 80005-119, 27241-249, 64980-737 +21Application ANDA217137, ANDA217529, ANDA217655 +12

Record updated 12 November 2026

Documents available

Documents that can be provided with this medicine. Your regulator may ask for more, and the quote lists the full set.

No document list is recorded for this medicine yet. Tell us which documents your regulator needs (for example a CoA, COPP or GMP certificate) when you request a quote.

Packs

Packs from every labeler of this generic presentation.

PackCodeLabelerMarketed since
50 mL in 1 bottle43386-500-11LupinIndia17 December 2012
50 mL in 1 bottle68180-150-01LupinIndia29 June 2010
50 mL in 1 bottle27241-249-49Ajanta PharmaIndia25 April 2022
50 mL in 1 bottle67877-775-89Ascend LaboratoriesIndia24 August 2023
50 mL in 1 bottle59651-701-50Aurobindo PharmaIndia9 July 2025
50 mL in 1 bottle70377-113-11BioconIndia1 September 2023
50 mL in 1 bottle31722-063-31Camber PharmaceuticalsIndia17 August 2023
50 mL in 1 bottle43598-572-11Dr. Reddy's LaboratoriesIndia15 March 2024
50 mL in 1 bottle42571-433-45Micro LabsIndia1 December 2023
55 mL in 1 bottle72205-233-84Novadoz PharmaceuticalsIndia16 August 2025
50 mL in 1 bottle, plastic68382-444-05Zydus LifesciencesIndia22 April 2021
50 mL in 1 bottle60219-2090-4Amneal Pharmaceuticals NY13 May 2024
50 mL in 1 bottle69238-2090-4Amneal Pharmaceuticals NY5 August 2022
50 mL in 1 bottle70954-316-10ANI Pharmaceuticals20 April 2021
50 mL in 1 bottle80005-119-16Carnegie Pharmaceuticals10 August 2023
55 mL in 1 bottle0527-5190-80Lannett2 June 2025
50 mL in 1 bottle, plastic68475-400-01Navinta22 April 2021
50 mL in 1 bottle64980-737-50Rising Pharma Holdings20 August 2026
100 mL in 1 bottle0832-6045-10Upsher-Smith Laboratories27 October 2023
150 mL in 1 bottle0832-6045-15Upsher-Smith Laboratories27 October 2023
50 mL in 1 bottle0832-6045-50Upsher-Smith Laboratories11 July 2023
50 mL in 1 bottle72603-171-01NorthStar Rx7 September 2023
50 mL in 1 bottle72603-564-01NorthStar Rx1 October 2026
50 mL in 1 bottle72162-2599-2Bryant Ranch Prepack9 January 2026
50 mL in 1 bottle51407-452-50Golden State Medical Supply19 May 2021
50 mL in 1 bottle81033-023-50Kesin Pharma25 November 2025

Status by register

Where this medicine is registered, from the source record and the regulator data we hold. Ask us about a country that is not listed.

RegisterStatusSource
US FDAListed, marketedSource record for this pageChecked 12 November 2026
US FDAFirst approved 15 October 1986Drugs@FDA
EU (EMA)Not recorded—
India (CDSCO)Not yet confirmed against CDSCO approval lists—
United StatesRegisteredUS FDA (NDC directory, openFDA)Checked 12 November 2026

Import route

Pick the destination country to see the legal import route, who applies and typical timelines, from our import guide for that country.

Import guides are available for 25 countries. Pick one to see its route summary.

BrazilColombiaEgyptEthiopiaGhanaIraqKazakhstanKenyaAll import guides

Other strengths and forms of Famotidine

Clinical summary

Famotidine is a histamine-2 receptor antagonist indicated in hospitalized adults, or as an alternative to oral famotidine in adults, for the treatment of active duodenal ulcer (DU), among other approved uses. MedsAcross supplies Famotidine 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

Read about Famotidine

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

Data sources

Need Famotidine 40 mg/5 mL powder for oral suspension for your hospital or patient?

Send one request with the destination country and quantity. We confirm availability, lead time and the documents your regulator needs.