Medicine
Caduet 10 mg/20 mg tablet
Caduet 10 mg/20 mg tablet is a prescription medicine containing Amlodipine and Atorvastatin for oral use, marketed by Pfizer Laboratories, 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
Export supply from India to licensed buyers
Typical lead time
On request
Counted from payment and complete documents
Shipping
Ambient
Store at 25°C (77°F), excursions permitted to 15°C -30°C (59°F -86°F).
Key facts
- Active ingredient (INN)
- Amlodipine and Atorvastatin
- Brand
- Caduet
- Strength
- 10 mg/20 mg
- Dosage form
- Tablet
- Route
- Oral
- Packs
- 30 tablets
- Marketing authorisation holder
- Pfizer Laboratories
- Manufacturers
- Pfizer LaboratoriesViatris Specialty
- Origin register
- US FDA, United States
- Storage
- Store at 25°C (77°F), excursions permitted to 15°C -30°C (59°F -86°F).
- Cold chain
- Not required on record
- Prescription status
- Prescription only
- Controlled substance
- Not recorded as controlled
- ATC code
- C10BX03 Amlodipine and Atorvastatin
- HS code (indicative)
- 3004.90Indicative only. Your customs broker confirms the final tariff code.
- Marketing category
- marketed
- Marketed since
- 31 August 2022
- Identifiers
- RxCUI 404011, 404013, 597967 +7DailyMed set ID 164394b3-d7ba-4bbf-b64b-e2dd15735ea8, 6f1a9bd8-ee30-4c7d-932f-3fa8c4e087b6NDC 58151-061, 0069-7232Application NDA021540
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
| Pack | Code | Labeler | Marketed since |
|---|---|---|---|
| 30 tablet, film coated in 1 bottle | 0069-7232-30 | Pfizer Laboratories | 31 August 2022 |
| 30 tablet, film coated in 1 bottle | 58151-061-93 | Viatris Specialty | 28 September 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.
| Register | Status | Source |
|---|---|---|
| US FDA | Listed, marketed | Source record for this pageChecked 12 November 2026 |
| US FDA | First approved 30 January 2004 | Drugs@FDA |
| EU (EMA) | Not recorded | — |
| India (CDSCO) | Not yet confirmed against CDSCO approval lists | — |
| United States | Registered | US 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 Amlodipine and Atorvastatin 10 mg/20 mg tablet.
Other strengths and forms of Amlodipine and Atorvastatin
Clinical summary
Amlodipine and Atorvastatin is a fixed-dose combination of a dihydropyridine calcium channel blocker, an HMG-CoA reductase inhibitor and a calcium channel blocker indicated in patients for whom treatment with both amlodipine and atorvastatin is appropriate. MedsAcross supplies Amlodipine and Atorvastatin 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 Amlodipine and AtorvastatinFor healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.
Data sources
- DailyMed label record · Checked 12 November 2026
- Caduet prescribing information (Viatris Specialty) · U.S. National Library of Medicine, DailyMed
Need Caduet 10 mg/20 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.