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United States· US:71335-2902_311870d0-0a69-4c33-9c1b-467cdb9a1e54

cholestyramine powder for suspension

A medicinal product containing cholestyramine, registered in United States by Bryant Ranch Prepack.

Checked against FDA National Drug Code directory (United States) on

Informational only — not a medical device.

SOURCE REGISTER · USFDA National Drug Code directory (Unite…normalisedcholestyramine powder for suspensionATC—REGISTER NO.US:71335-2902_311870d…PACKS LISTED1CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
CHOLESTYRAMINE
Manufacturer
Bryant Ranch Prepack
Country
United States (US)
ATC code
—
Reimbursed
Not published by this register
Source register
FDA National Drug Code directory (United States)
Last checked
September 27, 2026

Packs & prices · 1

  • ndc11
    71335-2902-1

Regulatory notes

No shortage, Orange Book or US label notes for this record.

Same medicine, other countries

Cholestyramine in 14 other countries

What each register calls a product with the same active substance — salts and hydrates count as the same.

All cholestyramine products

Authorised across Europe · EMA

The same active substance is authorised in 17 EEA countries. Names it is sold under:

  • Austria · Quantalan Zuckerfrei
  • Belgium · Questran
  • Cyprus · Resincolestiramina
  • Germany · Colestyramin 1 A Pharma, Colestyramin Ratiopharm
  • Denmark · Colestyramin Orifarm
  • Spain · Efensol, Resincolestiramina
  • Finland · Questran
  • France · Questran
  • United Kingdom (Northern Ireland) · Colestyramine Light Laboratorios Rubió, Colestyramine Neon Healthcare
  • Hungary · Cholestyramine
  • Ireland · Questran
  • Italy · Questran
  • Luxembourg · Questran
  • Netherlands · Colestyramine Suikervrij Focus, Questran
  • Norway · Questran, Questran Loc
  • Portugal · Quantalan
  • Sweden · Kolestyramin Alternova, Questran

Source: European Medicines Agency, Article 57 product data.

Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of FDA National Drug Code directory (United States). This is an informational data service and not a medical device — verify against the official source of record before any clinical decision.

For developers

The same record over the API, and the raw payload
GET /v1/drugs/ba59a949-4bf3-420a-90a0-325b7e06db7a
GET /v1/drugs/ba59a949-4bf3-420a-90a0-325b7e06db7a?format=fhir

Every response carries last_synced_at, so freshness is a field rather than a promise. Below is exactly what the ingestion wrote, before any presentation — the same JSON the API returns under payload.

{
  "route": "ORAL",
  "source": "ndc",
  "strength": "4",
  "substance": "CHOLESTYRAMINE",
  "productndc": "71335-2902",
  "dosage_form": "POWDER, FOR SUSPENSION",
  "dea_schedule": null,
  "strength_unit": "g/8.78g",
  "application_number": "ANDA211856",
  "marketing_category": "ANDA"
}

See everything about cholestyramine.

This page is the registration. A free account adds the label text as the regulator wrote it, what it costs per daily dose across the markets that publish a price, a feed of what changes in the registers, and an assistant that answers with its sources. Interaction severity is free; mechanism and management are on the Growth plan. No card, nothing to install.