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Medicine

Atazanavir 200 mg capsule

Atazanavir · Oral
Available on requestPrescription onlyUS FDAGeneric name

Atazanavir 200 mg capsule is a generic prescription medicine for oral use, made by 4 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 o to 25 • C (68 o to 77 • F).

Key facts

Active ingredient (INN)
Atazanavir
Brand
Sold under the generic name
Strength
200 mg
Dosage form
Capsule
Route
Oral
Packs
3 blister pack, 500 capsules, 180 capsules and 7 more
Manufacturers
Aurobindo PharmaIndiaCamber PharmaceuticalsIndiaLaurus LabsIndiaTeva Pharmaceuticals
Origin register
US FDA, United States
Storage
Store at 20 o to 25 • C (68 o to 77 • F).
Cold chain
Not required on record
Prescription status
Prescription only
Controlled substance
Not recorded as controlled
ATC code
J05AE08 Atazanavir
HS code (indicative)
3004.90Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
27 December 2017
Identifiers
RxCUI 402245, 402246, 402247 +1DailyMed set ID 7fbea274-d6b5-4faa-bbf0-05fefab42114, 8a0c609f-e296-4925-a35c-e93a04467655, c98e40ec-8a2c-4f19-b1c3-c82f708c2490 +1NDC 65862-712, 31722-654, 42385-921 +1Application ANDA204806, ANDA212278, ANDA212579 +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
3 blister pack in 1 carton / 10 capsule in 1 blister pack65862-712-03Aurobindo PharmaIndia25 June 2018
500 capsule in 1 bottle65862-712-05Aurobindo PharmaIndia25 June 2018
180 capsule in 1 bottle65862-712-18Aurobindo PharmaIndia25 June 2018
60 capsule in 1 bottle65862-712-60Aurobindo PharmaIndia25 June 2018
1000 capsule in 1 bottle31722-654-10Camber PharmaceuticalsIndia7 February 2022
100 blister pack in 1 carton / 10 capsule in 1 blister pack31722-654-31Camber PharmaceuticalsIndia7 February 2022
60 capsule in 1 bottle31722-654-60Camber PharmaceuticalsIndia7 February 2022
10 blister pack in 1 carton / 6 capsule in 1 blister pack42385-921-48Laurus LabsIndia30 April 2021
60 capsule in 1 bottle42385-921-60Laurus LabsIndia30 April 2021
60 capsule in 1 bottle0093-5527-06Teva Pharmaceuticals27 December 2017

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 20 June 2003Drugs@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 Atazanavir 200 mg capsule.

Compare 1

Other strengths and forms of Atazanavir

Clinical summary

Atazanavir is a protease inhibitor indicated in combination with other antiretroviral agents for the treatment of HIV-1 infection in adults and in pediatric patients 3 months and older weighing at least 5 kg, among other approved uses. MedsAcross supplies Atazanavir 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 Atazanavir

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

Data sources

Need Atazanavir 200 mg capsule 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.