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Medicine

Lamivudine and Zidovudine 150 mg/300 mg tablet

Available on requestPrescription onlyUS FDAGeneric name

Lamivudine and Zidovudine 150 mg/300 mg tablet is a generic prescription medicine for oral use, made by 7 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)
Lamivudine and Zidovudine
Brand
Sold under the generic name
Strength
150 mg/300 mg
Dosage form
Tablet
Route
Oral
Packs
500 tablets, 60 tablets, 100 tablets and 15 more
Manufacturers
Camber PharmaceuticalsIndiaAurobindo PharmaIndiaMacleods PharmaceuticalsIndiaBryant Ranch PrepackExelan PharmaceuticalsPD-Rx PharmaceuticalsXLCare Pharmaceuticals
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
J05AR01 Lamivudine and Zidovudine
HS code (indicative)
3004.90Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
6 February 2014
Identifiers
RxCUI 200082DailyMed set ID d40292ff-046c-4a04-b801-10768667951a, 55520835-0f24-4e52-af8c-d65841ccaba7, ff62c5fc-965d-4534-a571-a4f290cb9d83 +6NDC 65862-036, 72865-144, 43063-900 +6Application ANDA077558, ANDA203259, ANDA079124 +1

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
500 tablet, film coated in 1 bottle31722-506-05Camber PharmaceuticalsIndia18 September 2015
60 tablet, film coated in 1 bottle31722-506-60Camber PharmaceuticalsIndia18 September 2015
500 tablet, film coated in 1 bottle31722-739-05Camber PharmaceuticalsIndia6 February 2014
100 tablet, film coated in 1 blister pack31722-739-31Camber PharmaceuticalsIndia6 February 2014
60 tablet, film coated in 1 bottle31722-739-60Camber PharmaceuticalsIndia6 February 2014
6 blister pack in 1 carton / 10 tablet, film coated in 1 blister pack65862-036-10Aurobindo PharmaIndia5 May 2017
60 tablet, film coated in 1 bottle65862-036-60Aurobindo PharmaIndia5 May 2017
60 tablet in 1 bottle33342-003-09Macleods PharmaceuticalsIndia30 August 2018
500 tablet, film coated in 1 bottle76282-115-05Exelan Pharmaceuticals29 April 2015
60 tablet, film coated in 1 bottle76282-115-60Exelan Pharmaceuticals29 April 2015
60 tablet, film coated in 1 bottle72865-144-60XLCare Pharmaceuticals17 April 2020
6 tablet, film coated in 1 bottle71335-0639-1Bryant Ranch Prepack2 April 2021
60 tablet, film coated in 1 bottle71335-0639-2Bryant Ranch Prepack27 December 2021
4 tablet, film coated in 1 bottle71335-0639-3Bryant Ranch Prepack27 December 2021
6 tablet in 1 bottle71335-1916-1Bryant Ranch Prepack15 July 2021
60 tablet in 1 bottle71335-1916-2Bryant Ranch Prepack5 April 2024
4 tablet in 1 bottle71335-1916-3Bryant Ranch Prepack5 April 2024
6 tablet, film coated in 1 bottle, plastic43063-900-06PD-Rx Pharmaceuticals11 October 2018

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 26 September 1997Drugs@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 and Zidovudine 150 mg/300 mg tablet.

Compare 1

Clinical summary

Lamivudine and Zidovudine is a fixed-dose combination of a human immunodeficiency virus nucleoside analog reverse transcriptase inhibitor and a hepatitis B virus nucleoside analog reverse transcriptase inhibitor. It is available as tablets for oral use. MedsAcross supplies Lamivudine and Zidovudine 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 and Zidovudine

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

Data sources

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