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Medicine

Cholestyramine 4 g/5 g powder for oral suspension

Available on requestPrescription onlyUS FDAGeneric name

Cholestyramine 4 g/5 g powder for oral suspension is a generic prescription medicine for oral use, made by 2 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 between 20º to 25ºC (68º to 77ºF). Excursions permitted to 15º to 30ºC…

Key facts

Active ingredient (INN)
Cholestyramine
Brand
Sold under the generic name
Strength
4 g/5 g
Dosage form
Powder for oral suspension
Route
Oral
Packs
210 g, 60 packets and 2 more
Manufacturers
Par HealthBryant Ranch Prepack
Origin register
US FDA, United States
Storage
Store between 20º to 25ºC (68º to 77ºF). Excursions permitted to 15º to 30ºC (59º to 86ºF).
Cold chain
Not required on record
Prescription status
Prescription only
Controlled substance
Not recorded as controlled
ATC code
C10AC01 Cholestyramine
HS code (indicative)
3004.90Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
15 September 2005
Identifiers
RxCUI 848943, 1801279DailyMed set ID b0c65058-22c3-4f57-9b61-9bc6fcd6e240, c58d6bd9-0273-4c16-8533-495170413d8c, b26a13e9-42a2-4869-a00a-672bb1ac4742NDC 49884-466, 72162-1505, 63629-2162Application ANDA077203

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
210 g in 1 bottle49884-466-50Par Health24 April 2026
60 packet in 1 carton / 5 g in 1 packet49884-466-65Par Health15 September 2005
210 g in 1 can49884-466-67Par Health15 September 2005
210 g in 1 can63629-2162-1Bryant Ranch Prepack15 September 2005
210 g in 1 can72162-1505-2Bryant Ranch Prepack15 March 2024

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 3 August 1973Drugs@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 Cholestyramine 4 g/5 g powder for oral suspension.

Compare 1

Other strengths and forms of Cholestyramine

Clinical summary

Cholestyramine is a bile acid sequestrant indicated as adjunctive therapy to diet for the reduction of elevated serum cholesterol in patients with primary hypercholesterolemia (elevated low density lipoprotein [LDL] cholesterol) who do not respond adequately to diet. MedsAcross supplies Cholestyramine 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 Cholestyramine

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

Data sources

Need Cholestyramine 4 g/5 g powder for oral suspension 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.