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Medicine

Nitrofurantoin Mono 25 mg/75 mg capsule

Nitrofurantoin · Oral · PharmPak
Available on requestPrescription onlyUS FDA

Nitrofurantoin Mono 25 mg/75 mg capsule is a prescription medicine containing Nitrofurantoin for oral use, marketed by PharmPak, 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 controlled room temperature (59° to 86°F or 15° to 30°C).

Key facts

Active ingredient (INN)
Nitrofurantoin
Brand
Nitrofurantoin Mono
Strength
25 mg/75 mg
Dosage form
Capsule
Route
Oral
Packs
1 bottle
Marketing authorisation holder
PharmPak
Manufacturer
PharmPak
Origin register
US FDA, United States
Storage
Store at controlled room temperature (59° to 86°F or 15° to 30°C).
Cold chain
Not required on record
Prescription status
Prescription only
Controlled substance
Not recorded as controlled
ATC code
J01XE01 Nitrofurantoin
HS code (indicative)
3004.20Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
10 July 2019
Identifiers
RxCUI 1648755DailyMed set ID d9840719-271f-42a9-a5c9-3e039ec8fbacNDC 54348-849Application NDA020064

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

PackCodeLabelerMarketed since
1 bottle in 1 box / 6 capsule in 1 bottle54348-849-06PharmPak10 July 2019
1 bottle in 1 box / 10 capsule in 1 bottle54348-849-10PharmPak10 July 2019
1 bottle in 1 box / 14 capsule in 1 bottle54348-849-14PharmPak10 July 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 6 February 1953Drugs@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

Alternatives

Other makers and brands of Nitrofurantoin 25 mg/75 mg capsule.

Compare all 3

Other strengths and forms of Nitrofurantoin

Clinical summary

Nitrofurantoin is a nitrofuran antibacterial indicated in adults and pediatric patients 1 month of age and older for the treatment of urinary tract infections due to susceptible strains of Escherichia coli, Enterococcus species, Staphylococcus aureus. MedsAcross supplies Nitrofurantoin 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 Nitrofurantoin

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

Data sources

Need Nitrofurantoin Mono 25 mg/75 mg capsule 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.