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Medicine

Furosemide 40 mg tablet

Furosemide · Oral
Available on requestPrescription onlyUS FDAGeneric name

Furosemide 40 mg tablet is a generic prescription medicine for oral use, made by 28 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

Store at 20° -25° C (68° -77° F). Protect from light.

Key facts

Active ingredient (INN)
Furosemide
Brand
Sold under the generic name
Strength
40 mg
Dosage form
Tablet
Route
Oral
Packs
100 tablets, 1000 tablets, 10 tablets and 138 more
Manufacturers
Ipca LaboratoriesIndiaAurobindo PharmaIndiaA-S Medication SolutionsSolco HealthcareGranulation TechnologyHikma PharmaceuticalsLeading PharmaRising Pharma HoldingsCalvin ScottChartwell RX28 labelers on the register
Origin register
US FDA, United States
Storage
Store at 20° -25° C (68° -77° F). Protect from light.
Cold chain
Not required on record
Prescription status
Prescription only
Controlled substance
Not recorded as controlled
ATC code
C03CA01 Furosemide
HS code (indicative)
3004.90Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
10 November 1983
Identifiers
RxCUI 313988, 197732, 310429 +2DailyMed set ID 3f6529fb-1173-ada3-e063-6294a90a76cb, 020bc039-9e99-4895-96f8-0c6a556d3e67, b2cc89e5-6619-4113-ad31-48076652c856 +37NDC 71610-951, 72162-1361, 17224-185 +37Application ANDA077293, ANDA076796, ANDA216629 +5

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

A sample of 40 packs from 28 labelers. The register lists 141 packs for this generic presentation, and we confirm the exact pack on the quote.

PackCodeLabelerMarketed since
100 tablet in 1 bottle59651-797-01Aurobindo PharmaIndia17 July 2025
1000 tablet in 1 bottle59651-797-99Aurobindo PharmaIndia17 July 2025
100 tablet in 1 bottle83980-003-01Ipca LaboratoriesIndia3 June 2024
1000 tablet in 1 bottle83980-003-10Ipca LaboratoriesIndia3 June 2024
10 tablet in 1 bottle83980-003-97Ipca LaboratoriesIndia3 June 2024
100 tablet in 1 bottle0054-4299-25Hikma Pharmaceuticals10 November 1983
1000 tablet in 1 bottle0054-4299-31Hikma Pharmaceuticals10 November 1983
10 blister pack in 1 carton / 10 tablet in 1 blister pack0054-8299-25Hikma Pharmaceuticals10 November 1983
21 tablet in 1 bottle, plastic17224-185-21Calvin Scott15 May 2016
90 tablet in 1 package62135-754-90Chartwell RX17 April 2024
100 tablet in 1 bottle63561-0165-1Granulation Technology15 January 2026
1000 tablet in 1 bottle63561-0165-2Granulation Technology18 December 2025
90 tablet in 1 bottle63561-0165-9Granulation Technology18 December 2025
100 tablet in 1 bottle69315-117-01Leading Pharma15 May 2016
1000 tablet in 1 bottle69315-117-10Leading Pharma15 May 2016
100 tablet in 1 bottle64980-563-01Rising Pharma Holdings5 November 2022
1000 tablet in 1 bottle64980-563-10Rising Pharma Holdings5 November 2022
100 tablet in 1 bottle, plastic43547-402-10Solco Healthcare26 March 2004
1000 tablet in 1 bottle, plastic43547-402-11Solco Healthcare26 March 2004
5000 tablet in 1 bottle, plastic43547-402-51Solco Healthcare26 March 2004
1000000 tablet in 1 drum43547-402-94Solco Healthcare1 January 2022
30 tablet in 1 bottle50090-3313-0A-S Medication Solutions23 September 2021
100 tablet in 1 bottle50090-3313-1A-S Medication Solutions2 January 2018
60 tablet in 1 bottle50090-3313-3A-S Medication Solutions12 January 2022
90 tablet in 1 bottle50090-3313-9A-S Medication Solutions27 December 2017
100 tablet in 1 bottle50090-5702-0A-S Medication Solutions23 September 2021
180 tablet in 1 bottle50090-5702-1A-S Medication Solutions18 April 2023
30 tablet in 1 bottle50090-6646-0A-S Medication Solutions29 August 2023
100 tablet in 1 bottle50090-6646-1A-S Medication Solutions29 August 2023
60 tablet in 1 bottle50090-6646-3A-S Medication Solutions29 August 2023
90 tablet in 1 bottle50090-6646-9A-S Medication Solutions29 August 2023
180 tablet in 1 bottle50090-6647-1A-S Medication Solutions29 August 2023
90 tablet in 1 bottle50090-6937-0A-S Medication Solutions15 December 2023
30 tablet in 1 bottle50090-7703-0A-S Medication Solutions14 October 2025
100 tablet in 1 bottle50090-7703-1A-S Medication Solutions14 October 2025
60 tablet in 1 bottle50090-7703-3A-S Medication Solutions14 October 2025
90 tablet in 1 bottle50090-7703-9A-S Medication Solutions14 October 2025
180 tablet in 1 bottle50090-7704-1A-S Medication Solutions14 October 2025
90 tablet in 1 bottle50090-7705-0A-S Medication Solutions14 October 2025
100 tablet in 1 bottle68071-1809-1NuCare Pharmaceuticals,Inc29 January 2019

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 1 July 1966Drugs@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

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

Alternatives

Other makers and brands of Furosemide 40 mg tablet.

Compare 1

Other strengths and forms of Furosemide

Clinical summary

Furosemide is a loop diuretic indicated in adults and pediatric patients for the treatment of edema associated with congestive heart failure, cirrhosis of the liver, and renal disease, including the nephrotic syndrome. MedsAcross supplies Furosemide 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 Furosemide

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

Data sources

Need Furosemide 40 mg tablet 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.