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MedsAcross

Medicine

Crestor 20 mg tablet

Rosuvastatin · Oral · AstraZeneca Pharmaceuticals
Available on requestPrescription onlyUS FDA

Crestor 20 mg tablet is a prescription medicine containing Rosuvastatin for oral use, marketed by AstraZeneca Pharmaceuticals, 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 controlled room temperature, 20ºC to 25ºC (68ºF to 77ºF), excursions…

Key facts

Active ingredient (INN)
Rosuvastatin
Brand
Crestor
Strength
20 mg
Dosage form
Tablet
Route
Oral
Packs
90 tablets
Marketing authorisation holder
AstraZeneca Pharmaceuticals
Manufacturer
AstraZeneca Pharmaceuticals
Origin register
US FDA, United States
Storage
Store at controlled room temperature, 20ºC to 25ºC (68ºF to 77ºF), excursions permitted between 15°C and 30°C (59°F and 86°F). Protect from moisture.
Cold chain
Not required on record
Prescription status
Prescription only
Controlled substance
Not recorded as controlled
ATC code
C10AA07 Rosuvastatin
HS code (indicative)
3004.90Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
24 January 2022
Identifiers
RxCUI 859419, 859421, 859424 +5DailyMed set ID 325a5d0e-9a72-4015-9fcd-1655fb504ceeNDC 0310-7580Application NDA021366

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

PackCodeLabelerMarketed since
90 tablet, film coated in 1 bottle0310-7580-90AstraZeneca Pharmaceuticals24 January 2022

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 12 August 2003Drugs@FDA
EU (EMA)Not recorded—
India (CDSCO)Not yet confirmed against CDSCO approval lists—
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 Rosuvastatin 20 mg tablet.

Compare 1

Other strengths and forms of Rosuvastatin

Clinical summary

Rosuvastatin is an HMG-CoA reductase inhibitor indicated to reduce the risk of major adverse cardiovascular (CV) events (CV death, nonfatal myocardial infarction, nonfatal stroke, or an arterial revascularization procedure) in adults at increased risk for these events. MedsAcross supplies Rosuvastatin 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 Rosuvastatin

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

Data sources

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