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Medicine

Lamivudine 150 mg tablet

Lamivudine · Oral
Available on requestPrescription onlyUS FDAGeneric name

Lamivudine 150 mg tablet is a generic prescription medicine for oral use, made by 11 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 LAMIVUDINE Tablets at 25°C (77°F), excursions permitted to 15° to 30°C…

Key facts

Active ingredient (INN)
Lamivudine
Brand
Sold under the generic name
Strength
150 mg
Dosage form
Tablet
Route
Oral
Packs
6 blister pack, 60 tablets, 600 tablets and 12 more
Manufacturers
Camber PharmaceuticalsIndiaAurobindo PharmaIndiaMacleods PharmaceuticalsIndiaStrides PharmaIndiaApotexAmerican Health PackagingCouplerGolden State Medical SupplyIngenus PharmaceuticalsMajor Pharmaceuticals11 labelers on the register
Origin register
US FDA, United States
Storage
Store LAMIVUDINE Tablets at 25°C (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
J05AF05 Lamivudine
HS code (indicative)
3004.90Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
2 December 2011
Identifiers
RxCUI 199147, 349491DailyMed set ID 47f8be59-178c-4bad-96a4-a5c82784f308, f3637209-303e-4232-ae79-07315a990973, 2d7db3b2-9b3c-3031-e063-6294a90a342c +8NDC 50742-623, 60429-353, 67046-1459 +8Application ANDA206974, ANDA091606, ANDA090457 +4

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
6 blister pack in 1 carton / 10 tablet, film coated in 1 blister pack65862-025-10Aurobindo PharmaIndia21 November 2016
60 tablet, film coated in 1 bottle65862-025-60Aurobindo PharmaIndia21 November 2016
600 tablet, film coated in 1 bottle31722-753-06Camber PharmaceuticalsIndia6 January 2014
10 tablet, film coated in 1 blister pack31722-753-31Camber PharmaceuticalsIndia6 January 2014
100 tablet, film coated in 1 carton31722-753-32Camber PharmaceuticalsIndia6 January 2014
60 tablet, film coated in 1 bottle31722-753-60Camber PharmaceuticalsIndia6 January 2014
60 tablet, film coated in 1 bottle33342-001-09Macleods PharmaceuticalsIndia2 May 2019
60 tablet, film coated in 1 bottle64380-710-03Strides PharmaIndia19 October 2018
60 tablet, film coated in 1 bottle60505-3251-6Apotex2 December 2011
1000 tablet, film coated in 1 bottle60505-3251-8Apotex2 December 2011
60 tablet in 1 bottle, plastic50742-623-60Ingenus Pharmaceuticals1 February 2017
30 blister pack in 1 carton / 1 tablet, film coated in 1 blister pack60687-720-21American Health Packaging19 January 2023
30 tablet, film coated in 1 blister pack67046-1459-3Coupler6 February 2025
60 tablet, film coated in 1 bottle60429-353-60Golden State Medical Supply2 December 2011
30 blister pack in 1 carton / 1 tablet, film coated in 1 blister pack0904-6583-04Major Pharmaceuticals2 December 2011

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 17 November 1995Drugs@FDA
EU (EMA)AuthorisedEMA medicines data
India (CDSCO)Not yet confirmed against CDSCO approval lists—
AustriaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
BelgiumRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
BulgariaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
CroatiaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
CyprusRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
CzechiaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
DenmarkRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
EstoniaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
FinlandRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
FranceRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
GermanyRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
GreeceRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
HungaryRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
IcelandRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
IrelandRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
ItalyRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LatviaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LiechtensteinRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LithuaniaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LuxembourgRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
MaltaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
NetherlandsRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
NorwayRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
PolandRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
PortugalRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
RomaniaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SlovakiaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SloveniaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SpainRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SwedenRegisteredEuropean 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 Lamivudine 150 mg tablet.

Compare 1

Other strengths and forms of Lamivudine

Clinical summary

Lamivudine is a hepatitis B virus nucleoside analog reverse transcriptase inhibitor indicated in combination with other antiretroviral agents for the treatment of human immunodeficiency virus type 1 (HIV-1) infection. It is available as tablets and oral solution. MedsAcross supplies Lamivudine 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 Lamivudine

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

Data sources

Need Lamivudine 150 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.