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Medicine

Naproxen 275 mg tablet

Naproxen · Oral
Available on requestPrescription onlyUS FDAGeneric name

Naproxen 275 mg tablet is a generic prescription medicine for oral use, made by 6 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°C to 25°C (68°F to 77°F) in well-closed containers.

Key facts

Active ingredient (INN)
Naproxen
Brand
Sold under the generic name
Strength
275 mg
Dosage form
Tablet
Route
Oral
Packs
100 tablets, 500 tablets, 1000 tablets and 20 more
Manufacturers
Dr. Reddy's LaboratoriesIndiaAurobindo PharmaIndiaGlenmark PharmaceuticalsIndiaBryant Ranch PrepackAsclemedScieGen Pharmaceuticals
Origin register
US FDA, United States
Storage
Store at 20°C to 25°C (68°F to 77°F) in well-closed containers.
Cold chain
Not required on record
Prescription status
Prescription only
Controlled substance
Not recorded as controlled
ATC code
G02CC02 Naproxen
HS code (indicative)
3004.90Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
1 August 2007
Identifiers
RxCUI 849398, 849431, 198012 +2DailyMed set ID 37de42a6-701b-7f6e-e631-519e2ea78b54, 79f48c92-783d-40f2-9865-89958a9f9de6, b0571e62-9330-438d-a2ba-873477f52dc4 +3NDC 43598-494, 50228-432, 76420-637 +3Application ANDA078486, ANDA212199, ANDA200629 +1

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
100 tablet, film coated in 1 bottle65862-515-01Aurobindo PharmaIndia31 October 2011
500 tablet, film coated in 1 bottle65862-515-05Aurobindo PharmaIndia31 October 2011
1000 tablet, film coated in 1 bottle65862-515-99Aurobindo PharmaIndia31 October 2011
100 tablet, film coated in 1 bottle43598-494-01Dr. Reddy's LaboratoriesIndia26 April 2016
500 tablet, film coated in 1 bottle43598-494-05Dr. Reddy's LaboratoriesIndia26 April 2016
1000 tablet, film coated in 1 bottle43598-494-10Dr. Reddy's LaboratoriesIndia26 April 2016
30 tablet, film coated in 1 bottle43598-494-30Dr. Reddy's LaboratoriesIndia26 April 2016
100 tablet in 1 bottle68462-178-01Glenmark PharmaceuticalsIndia1 August 2007
500 tablet in 1 bottle68462-178-05Glenmark PharmaceuticalsIndia1 August 2007
100 tablet in 1 bottle50228-432-01ScieGen Pharmaceuticals30 October 2019
500 tablet in 1 bottle50228-432-05ScieGen Pharmaceuticals30 October 2019
1000 tablet in 1 bottle50228-432-10ScieGen Pharmaceuticals30 October 2019
30 tablet in 1 bottle50228-432-30ScieGen Pharmaceuticals30 October 2019
100 tablet in 1 bottle76420-637-01Asclemed18 October 2023
30 tablet in 1 bottle76420-637-30Asclemed18 October 2023
60 tablet in 1 bottle76420-637-60Asclemed18 October 2023
90 tablet in 1 bottle76420-637-90Asclemed18 October 2023
60 tablet, film coated in 1 bottle71335-1925-1Bryant Ranch Prepack30 January 2025
90 tablet, film coated in 1 bottle71335-1925-2Bryant Ranch Prepack30 January 2025
42 tablet, film coated in 1 bottle71335-1925-3Bryant Ranch Prepack30 January 2025
20 tablet, film coated in 1 bottle71335-1925-4Bryant Ranch Prepack30 January 2025
120 tablet, film coated in 1 bottle71335-1925-5Bryant Ranch Prepack30 January 2025
30 tablet, film coated in 1 bottle71335-1925-6Bryant Ranch Prepack29 July 2021

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 11 March 1976Drugs@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 Naproxen

Clinical summary

Naproxen is a nonsteroidal anti-inflammatory drug indicated for the relief of the signs and symptoms of. It is available as tablets, delayed-release tablets and extended-release tablets for oral use. MedsAcross supplies Naproxen 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 Naproxen

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

Data sources

Need Naproxen 275 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.