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MedsAcross

Medicine

Mesalamine 800 mg delayed-release tablet

Mesalamine · Oral
Available on requestPrescription onlyUS FDAGeneric name

Mesalamine 800 mg delayed-release tablet is a generic prescription medicine for oral use, made by 5 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). Protect from moisture.

Key facts

Active ingredient (INN)
Mesalamine
Brand
Sold under the generic name
Strength
800 mg
Dosage form
Delayed-release tablet
Route
Oral
Packs
180 tablets, 10 blister pack, 30 blister pack and 5 more
Manufacturers
Zydus LifesciencesIndiaAmerican Health PackagingAmneal PharmaceuticalsAvKARETeva Pharmaceuticals
Origin register
US FDA, United States
Storage
Store at 20°C to 25°C (68°F to 77°F). Protect from moisture.
Cold chain
Not required on record
Prescription status
Prescription only
Controlled substance
Not recorded as controlled
ATC code
A07EC02 Mesalamine
HS code (indicative)
3004.90Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
2 August 2018
Identifiers
RxCUI 833234DailyMed set ID ad8c7930-92e2-4372-a874-da22b9ae333e, 00f77203-3615-47e8-ae25-6e1cf8a2a00a, 52d96501-47f3-45d8-a181-98763b9f8965 +3NDC 68382-435, 65162-360, 70771-1110 +3Application ANDA203286, ANDA215067, ANDA213191

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
180 tablet, delayed release in 1 bottle68382-435-28Zydus LifesciencesIndia2 August 2018
10 blister pack in 1 carton / 10 tablet, delayed release in 1 blister pack68382-435-77Zydus LifesciencesIndia2 August 2018
10 blister pack in 1 carton / 10 tablet, delayed release in 1 blister pack70771-1110-4Zydus LifesciencesIndia2 August 2018
180 tablet, delayed release in 1 bottle70771-1110-8Zydus LifesciencesIndia2 August 2018
180 tablet, delayed release in 1 bottle65162-360-18Amneal Pharmaceuticals19 February 2025
180 tablet, delayed release in 1 bottle0480-7750-80Teva Pharmaceuticals22 August 2024
30 blister pack in 1 box, unit-dose / 1 tablet, delayed release in 1 blister pack60687-408-25American Health Packaging17 April 2019
180 tablet, delayed release in 1 bottle42291-489-18AvKARE25 September 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 24 December 1987Drugs@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 Mesalamine

Clinical summary

Mesalamine is an aminosalicylate indicated for the treatment of active mild to moderate distal ulcerative colitis, proctosigmoiditis or proctitis in adults. It is available as delayed-release tablets, extended-release capsules and suppositories for oral and rectal use. MedsAcross supplies Mesalamine 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 Mesalamine

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

Data sources

Need Mesalamine 800 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.