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Medicine

Felodipine 5 mg extended-release tablet

Felodipine · Oral
Available on requestPrescription onlyUS FDAGeneric name

Felodipine 5 mg extended-release tablet is a generic prescription medicine for oral use, made by 10 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° to 25°C (68° to 77°F). Protect from light.

Key facts

Active ingredient (INN)
Felodipine
Brand
Sold under the generic name
Strength
5 mg
Dosage form
Extended-release tablet
Route
Oral
Packs
100 tablets, 90 tablets, 1000 tablets and 21 more
Manufacturers
Torrent PharmaceuticalsIndiaGlenmark PharmaceuticalsIndiaAurobindo PharmaIndiaAvet PharmaceuticalsIndiaBryant Ranch PrepackPar HealthYiling PharmaceuticalChartwell RXRising Pharma HoldingsWestminster Pharmaceuticals
Origin register
US FDA, United States
Storage
Store at 20° to 25°C (68° to 77°F). Protect from light.
Cold chain
Not required on record
Prescription status
Prescription only
Controlled substance
Not recorded as controlled
ATC code
C08CA02 Felodipine
HS code (indicative)
3004.90Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
20 December 2010
Identifiers
RxCUI 402695, 402696, 402698DailyMed set ID 0bef7cf2-012b-4804-ac93-0a8b333035db, 05feb0a1-8a0c-4d8a-9b86-5e700ea6fd64, fddebfce-70ed-4ee1-8598-bbb8f1ca9263 +10NDC 23155-049, 63629-2195, 62135-647 +10Application ANDA201964, ANDA200815, ANDA210847 +3

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, extended release in 1 bottle65862-674-01Aurobindo PharmaIndia17 January 2013
90 tablet, film coated, extended release in 1 bottle65862-674-90Aurobindo PharmaIndia17 January 2013
1000 tablet, film coated, extended release in 1 bottle65862-674-99Aurobindo PharmaIndia17 January 2013
100 tablet, extended release in 1 bottle23155-049-01Avet PharmaceuticalsIndia8 November 2013
100 tablet, film coated, extended release in 1 bottle68462-234-01Glenmark PharmaceuticalsIndia20 December 2010
1000 tablet, film coated, extended release in 1 bottle68462-234-10Glenmark PharmaceuticalsIndia20 December 2010
10 blister pack in 1 carton / 10 tablet, film coated, extended release in 1 blister pack68462-234-11Glenmark PharmaceuticalsIndia20 December 2010
90 tablet, film coated, extended release in 1 bottle68462-234-90Glenmark PharmaceuticalsIndia20 December 2010
100 tablet, extended release in 1 bottle13668-133-01Torrent PharmaceuticalsIndia28 November 2011
500 tablet, extended release in 1 bottle13668-133-05Torrent PharmaceuticalsIndia28 November 2011
1000 tablet, extended release in 1 bottle13668-133-10Torrent PharmaceuticalsIndia28 November 2011
30 tablet, extended release in 1 bottle13668-133-30Torrent PharmaceuticalsIndia28 November 2011
90 tablet, extended release in 1 bottle13668-133-90Torrent PharmaceuticalsIndia28 November 2011
90 tablet, extended release in 1 bottle62135-647-90Chartwell RX5 June 2023
100 tablet, extended release in 1 bottle, plastic0603-3582-21Par Health15 December 2011
500 tablet, extended release in 1 bottle, plastic0603-3582-28Par Health15 December 2011
100 tablet, film coated, extended release in 1 bottle57237-109-01Rising Pharma Holdings17 January 2013
100 tablet, extended release in 1 bottle69117-0029-1Yiling Pharmaceutical1 August 2019
500 tablet, extended release in 1 bottle69117-0029-2Yiling Pharmaceutical1 August 2019
100 tablet, extended release in 1 bottle, plastic63629-2195-1Bryant Ranch Prepack12 March 2021
500 tablet, extended release in 1 bottle, plastic63629-2196-1Bryant Ranch Prepack15 December 2011
30 tablet, film coated, extended release in 1 bottle71335-1318-1Bryant Ranch Prepack27 August 2019
30 tablet, film coated, extended release in 1 bottle71335-1486-1Bryant Ranch Prepack21 January 2020
100 tablet, extended release in 1 bottle69367-265-01Westminster Pharmaceuticals31 March 2023

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 25 July 1991Drugs@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 Felodipine

Clinical summary

Felodipine is a dihydropyridine calcium channel blocker indicated for the treatment of hypertension, to lower blood pressure. It is available as extended-release tablets and tablets for oral use. MedsAcross supplies Felodipine 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 Felodipine

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

Data sources

Need Felodipine 5 mg extended-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.