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Medicine

Esomeprazole and Naproxen 20 mg/500 mg delayed-release tablet

Available on requestPrescription onlyUS FDAGeneric name

Esomeprazole and Naproxen 20 mg/500 mg delayed-release tablet is a generic prescription medicine for oral use, made by 9 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),. Store in the original container and keep the…

Key facts

Active ingredient (INN)
Esomeprazole and Naproxen
Brand
Sold under the generic name
Strength
20 mg/500 mg
Dosage form
Delayed-release tablet
Route
Oral
Packs
60 tablets, 500 tablets, 30 tablets and 25 more
Manufacturers
Ajanta PharmaIndiaDr. Reddy's LaboratoriesIndiaBryant Ranch PrepackPhoenix RXAsclemedPreferred PharmaceuticalsScieGen PharmaceuticalsProficient RxDoc Rx
Origin register
US FDA, United States
Storage
Store at 20°-25°C (68°-77°F),. Store in the original container and keep the bottle tightly closed to protect from moisture.
Cold chain
Not required on record
Prescription status
Prescription only
Controlled substance
Not recorded as controlled
ATC code
M01AE52 Esomeprazole and Naproxen
HS code (indicative)
3004.90Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
18 February 2020
Identifiers
RxCUI 994005, 994008DailyMed set ID 7b3af5a8-0c92-43f4-af13-7a47dca20e92, 7ca657dc-4376-4693-8568-99351fac8186, 1ef3fe94-9bbb-934d-a09b-d19a1d23a4d5 +11NDC 76420-889, 27241-203, 55111-701 +11Application ANDA204206, ANDA213699, ANDA217738

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
60 tablet, delayed release in 1 bottle27241-203-60Ajanta PharmaIndia6 October 2022
60 tablet, delayed release in 1 bottle55111-701-60Dr. Reddy's LaboratoriesIndia18 February 2020
60 tablet, delayed release in 1 bottle69306-005-60Doc Rx27 May 2026
500 tablet, delayed release in 1 bottle50228-438-05ScieGen Pharmaceuticals11 October 2023
30 tablet, delayed release in 1 bottle50228-438-30ScieGen Pharmaceuticals11 October 2023
60 tablet, delayed release in 1 bottle50228-438-60ScieGen Pharmaceuticals12 March 2024
60 tablet, delayed release in 1 bottle63629-4873-1Bryant Ranch Prepack17 January 2025
30 tablet, delayed release in 1 bottle63629-4873-2Bryant Ranch Prepack17 January 2025
60 tablet, delayed release in 1 bottle71335-2552-1Bryant Ranch Prepack21 January 2025
30 tablet, delayed release in 1 bottle71335-2552-2Bryant Ranch Prepack21 January 2025
60 tablet, delayed release in 1 bottle71335-2553-1Bryant Ranch Prepack23 January 2025
30 tablet, delayed release in 1 bottle71335-2553-2Bryant Ranch Prepack23 January 2025
60 tablet, delayed release in 1 bottle85509-1203-1Phoenix RX1 August 2025
30 tablet, delayed release in 1 bottle85509-1203-3Phoenix RX21 July 2025
100 tablet, delayed release in 1 bottle85509-1438-1Phoenix RX3 March 2026
30 tablet, delayed release in 1 bottle85509-1438-3Phoenix RX3 March 2026
60 tablet, delayed release in 1 bottle85509-1438-6Phoenix RX3 March 2026
90 tablet, delayed release in 1 bottle85509-1438-9Phoenix RX3 March 2026
30 tablet, delayed release in 1 bottle68788-4043-3Preferred Pharmaceuticals17 October 2025
60 tablet, delayed release in 1 bottle68788-4043-6Preferred Pharmaceuticals17 October 2025
30 tablet, delayed release in 1 bottle68788-8766-3Preferred Pharmaceuticals8 November 2024
60 tablet, delayed release in 1 bottle68788-8766-6Preferred Pharmaceuticals8 November 2024
60 tablet, delayed release in 1 bottle82804-276-60Proficient Rx31 March 2026
60 tablet, delayed release in 1 bottle82804-303-60Proficient Rx16 July 2026
100 tablet, delayed release in 1 bottle76420-889-01Asclemed28 December 2024
30 tablet, delayed release in 1 bottle76420-889-30Asclemed28 December 2024
60 tablet, delayed release in 1 bottle76420-889-60Asclemed28 December 2024
90 tablet, delayed release in 1 bottle76420-889-90Asclemed28 December 2024

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 30 April 2010Drugs@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 Esomeprazole and Naproxen

Clinical summary

Esomeprazole and Naproxen is a fixed-dose combination of a nonsteroidal anti-inflammatory drug and a proton pump inhibitor indicated in adult and adolescent patients 12 years of age and older weighing at least 38 kg. MedsAcross supplies Esomeprazole and 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 Esomeprazole and Naproxen

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

Data sources

Need Esomeprazole and Naproxen 20 mg/500 mg delayed-release 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.