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Medicine

Desvenlafaxine 100 mg extended-release tablet

Available on requestPrescription onlyUS FDAGeneric name

Desvenlafaxine 100 mg extended-release tablet is a generic prescription medicine for oral use, made by 15 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), excursions permitted to 15° to 30°C (59°…

Key facts

Active ingredient (INN)
Desvenlafaxine
Brand
Sold under the generic name
Strength
100 mg
Dosage form
Extended-release tablet
Route
Oral
Packs
30 tablets, 90 tablets, 100 tablets and 61 more
Manufacturers
Alembic PharmaceuticalsIndiaMacleods PharmaceuticalsIndiaSun Pharmaceutical IndustriesIndiaLupinIndiaBryant Ranch PrepackBreckenridge PharmaceuticalAdvagen PharmaHikma PharmaceuticalsSlate Run PharmaceuticalsActavis Pharma15 labelers on the register
Origin register
US FDA, United States
Storage
Store at 20° to 25°C (68° to 77°F), excursions permitted to 15° to 30°C (59° to 86°F).
Cold chain
Not required on record
Prescription status
Prescription only
Controlled substance
Not recorded as controlled
ATC code
N06AX23 Desvenlafaxine
HS code (indicative)
3004.90Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
5 March 2013
Identifiers
RxCUI 1874553, 1607617, 1874559 +2DailyMed set ID 325be002-4db2-40e9-e063-6394a90ae94e, 44f4b928-d5b8-44e7-bfa6-81fb0dc1a718, 91cf39c9-4d26-480a-a3a3-a3d8d4c4d222 +17NDC 67046-1545, 70436-013, 63304-192 +17Application ANDA204003, ANDA210014, NDA204150 +6

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

A sample of 40 packs from 15 labelers. The register lists 64 packs for this generic presentation, and we confirm the exact pack on the quote.

PackCodeLabelerMarketed since
30 tablet, extended release in 1 bottle46708-153-30Alembic PharmaceuticalsIndia5 March 2013
90 tablet, extended release in 1 bottle46708-153-90Alembic PharmaceuticalsIndia5 March 2013
100 tablet, extended release in 1 carton46708-541-10Alembic PharmaceuticalsIndia1 March 2017
14 tablet, extended release in 1 bottle46708-541-17Alembic PharmaceuticalsIndia1 March 2017
30 tablet, extended release in 1 bottle46708-541-30Alembic PharmaceuticalsIndia1 March 2017
100 tablet, extended release in 1 bottle46708-541-31Alembic PharmaceuticalsIndia1 March 2017
80 tablet, extended release in 1 carton46708-541-80Alembic PharmaceuticalsIndia1 March 2017
90 tablet, extended release in 1 bottle46708-541-90Alembic PharmaceuticalsIndia1 March 2017
1000 tablet, extended release in 1 bottle46708-541-91Alembic PharmaceuticalsIndia1 March 2017
30 tablet, film coated, extended release in 1 bottle68180-593-06LupinIndia1 March 2017
30 tablet, extended release in 1 bottle33342-389-07Macleods PharmaceuticalsIndia16 June 2018
90 tablet, extended release in 1 bottle33342-389-10Macleods PharmaceuticalsIndia16 June 2018
10 blister pack in 1 carton / 10 tablet, extended release in 1 blister pack33342-389-12Macleods PharmaceuticalsIndia16 June 2018
30 tablet, extended release in 1 bottle63304-192-30Sun Pharmaceutical IndustriesIndia5 March 2013
90 tablet, extended release in 1 bottle63304-192-90Sun Pharmaceutical IndustriesIndia5 March 2013
30 tablet, extended release in 1 bottle0591-3660-30Actavis Pharma1 March 2017
1000 tablet, extended release in 1 package72888-144-00Advagen Pharma31 January 2022
500 tablet, extended release in 1 package72888-144-05Advagen Pharma31 January 2022
30 tablet, extended release in 1 package72888-144-30Advagen Pharma31 January 2022
90 tablet, extended release in 1 package72888-144-90Advagen Pharma31 January 2022
100 tablet, extended release in 1 bottle51991-312-01Breckenridge Pharmaceutical1 March 2017
1000 tablet, extended release in 1 bottle51991-312-10Breckenridge Pharmaceutical1 March 2017
100 tablet, extended release in 1 carton51991-312-11Breckenridge Pharmaceutical1 March 2017
14 tablet, extended release in 1 bottle51991-312-14Breckenridge Pharmaceutical1 March 2017
30 tablet, extended release in 1 bottle51991-312-33Breckenridge Pharmaceutical1 March 2017
80 tablet, extended release in 1 carton51991-312-80Breckenridge Pharmaceutical1 March 2017
90 tablet, extended release in 1 bottle51991-312-90Breckenridge Pharmaceutical1 March 2017
30 tablet, film coated, extended release in 1 bottle0054-0401-13Hikma Pharmaceuticals1 March 2017
90 tablet, film coated, extended release in 1 bottle0054-0401-22Hikma Pharmaceuticals1 March 2017
30 tablet, extended release in 1 bottle, plastic70436-013-04Slate Run Pharmaceuticals1 August 2020
90 tablet, extended release in 1 bottle, plastic70436-013-06Slate Run Pharmaceuticals1 August 2020
30 tablet, extended release in 1 bottle63629-7559-1Bryant Ranch Prepack19 March 2018
28 tablet, extended release in 1 bottle63629-7559-2Bryant Ranch Prepack29 October 2024
90 tablet, extended release in 1 bottle63629-7559-3Bryant Ranch Prepack25 August 2021
60 tablet, extended release in 1 bottle63629-7559-4Bryant Ranch Prepack29 October 2024
30 tablet, film coated, extended release in 1 bottle71335-1331-1Bryant Ranch Prepack3 September 2019
28 tablet, film coated, extended release in 1 bottle71335-1331-2Bryant Ranch Prepack20 May 2024
90 tablet, film coated, extended release in 1 bottle71335-1331-3Bryant Ranch Prepack20 May 2024
60 tablet, film coated, extended release in 1 bottle71335-1331-4Bryant Ranch Prepack20 May 2024
30 tablet, extended release in 1 bottle, plastic71335-1815-1Bryant Ranch Prepack17 July 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 29 February 2008Drugs@FDA
EU (EMA)Application withdrawnEMA medicines data
India (CDSCO)Not yet confirmed against CDSCO approval lists—
AustriaWithdrawnEuropean Medicines Agency (central authorisation)Checked 12 November 2026
BelgiumWithdrawnEuropean Medicines Agency (central authorisation)Checked 12 November 2026
BulgariaWithdrawnEuropean Medicines Agency (central authorisation)Checked 12 November 2026
CroatiaWithdrawnEuropean Medicines Agency (central authorisation)Checked 12 November 2026
CyprusWithdrawnEuropean Medicines Agency (central authorisation)Checked 12 November 2026
CzechiaWithdrawnEuropean Medicines Agency (central authorisation)Checked 12 November 2026
DenmarkWithdrawnEuropean Medicines Agency (central authorisation)Checked 12 November 2026
EstoniaWithdrawnEuropean Medicines Agency (central authorisation)Checked 12 November 2026
FinlandWithdrawnEuropean Medicines Agency (central authorisation)Checked 12 November 2026
FranceWithdrawnEuropean Medicines Agency (central authorisation)Checked 12 November 2026
GermanyWithdrawnEuropean Medicines Agency (central authorisation)Checked 12 November 2026
GreeceWithdrawnEuropean Medicines Agency (central authorisation)Checked 12 November 2026
HungaryWithdrawnEuropean Medicines Agency (central authorisation)Checked 12 November 2026
IcelandWithdrawnEuropean Medicines Agency (central authorisation)Checked 12 November 2026
IrelandWithdrawnEuropean Medicines Agency (central authorisation)Checked 12 November 2026
ItalyWithdrawnEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LatviaWithdrawnEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LiechtensteinWithdrawnEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LithuaniaWithdrawnEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LuxembourgWithdrawnEuropean Medicines Agency (central authorisation)Checked 12 November 2026
MaltaWithdrawnEuropean Medicines Agency (central authorisation)Checked 12 November 2026
NetherlandsWithdrawnEuropean Medicines Agency (central authorisation)Checked 12 November 2026
NorwayWithdrawnEuropean Medicines Agency (central authorisation)Checked 12 November 2026
PolandWithdrawnEuropean Medicines Agency (central authorisation)Checked 12 November 2026
PortugalWithdrawnEuropean Medicines Agency (central authorisation)Checked 12 November 2026
RomaniaWithdrawnEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SlovakiaWithdrawnEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SloveniaWithdrawnEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SpainWithdrawnEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SwedenWithdrawnEuropean Medicines Agency (central authorisation)Checked 12 November 2026
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 Desvenlafaxine 100 mg extended-release tablet.

Compare 1

Other strengths and forms of Desvenlafaxine

Clinical summary

Desvenlafaxine is a serotonin and norepinephrine reuptake inhibitor indicated for the treatment of adults with major depressive disorder (MDD). It is available as extended-release tablets for oral use. MedsAcross supplies Desvenlafaxine 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 Desvenlafaxine

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

Data sources

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Send one request with the destination country and quantity. We confirm availability, lead time and the documents your regulator needs.