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Medicine

Maraviroc 300 mg tablet

Maraviroc · Oral
Available on requestPrescription onlyUS FDAGeneric name

Maraviroc 300 mg tablet is a generic prescription medicine for oral use, made by 8 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

Bottle of 60 tablets (NDC 31722-580-60) Maraviroc film-coated tablets should…

Key facts

Active ingredient (INN)
Maraviroc
Brand
Sold under the generic name
Strength
300 mg
Dosage form
Tablet
Route
Oral
Packs
60 tablets and 5 more
Manufacturers
Camber PharmaceuticalsIndiaZydus LifesciencesIndiaA-S Medication SolutionsA2A Integrated Pharmaceuticalsi3 PharmaceuticalsNavintaRhodes PharmaceuticalsXLCare Pharmaceuticals
Origin register
US FDA, United States
Storage
Bottle of 60 tablets (NDC 31722-580-60) Maraviroc film-coated tablets should be stored at 20° to 25°C (68° to 77°F).
Cold chain
Not required on record
Prescription status
Prescription only
Controlled substance
Not recorded as controlled
ATC code
J05AX09 Maraviroc
HS code (indicative)
3004.90Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
6 February 2022
Identifiers
RxCUI 728223, 728225DailyMed set ID 09ec3e79-c0d3-4b8f-80d8-0a854c4ca339, c35f72dc-d90e-43f8-9899-f7d1da89460d, 9bba17ba-0bc5-430c-96d1-c568e236a0ed +5NDC 31722-580, 42858-247, 70710-1931 +5Application ANDA203347, ANDA216143, ANDA217880 +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
60 tablet, film coated in 1 bottle31722-580-60Camber PharmaceuticalsIndia6 February 2022
60 tablet, film coated in 1 bottle70710-1931-6Zydus LifesciencesIndia23 May 2025
60 tablet, film coated in 1 bottle73141-025-02A2A Integrated Pharmaceuticals16 May 2024
60 tablet, film coated in 1 bottle72319-025-02i3 Pharmaceuticals15 September 2023
60 tablet, film coated in 1 bottle68475-007-01Navinta23 June 2025
60 tablet, film coated in 1 bottle, plastic42858-247-06Rhodes Pharmaceuticals30 September 2026
60 tablet, film coated in 1 bottle72865-232-60XLCare Pharmaceuticals1 June 2023
60 tablet, film coated in 1 bottle50090-8005-0A-S Medication Solutions25 June 2026

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 6 August 2007Drugs@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 Maraviroc 300 mg tablet.

Compare 1

Other strengths and forms of Maraviroc

Clinical summary

Maraviroc is a CCR5 Co-receptor antagonist indicated in combination with other antiretroviral agents for the treatment of only CCR5-tropic human immunodeficiency virus type 1 (HIV-1) infection in adult and pediatric patients weighing at least 2 kg. MedsAcross supplies Maraviroc 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 Maraviroc

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

Data sources

Need Maraviroc 300 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.