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CHOLESTYRAMINE

NDC 70771-1070 · Zydus Lifesciences Limited

Generic nameCHOLESTYRAMINE
Dosage formPOWDER, FOR SUSPENSION
RouteORAL
Active ingredient(s)CHOLESTYRAMINE
Strength4 g/5.5g
Pharmacologic classBile Acid Sequestrant [EPC], Bile-acid Binding Activity [MoA]
Marketing categoryANDA

Packages

70771-1070-1 — 231 g in 1 CONTAINER (70771-1070-1)

70771-1070-2 — 60 POUCH in 1 CARTON (70771-1070-2) / 5.5 g in 1 POUCH

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

49884-937 — Cholestyramine, 51224-009 — Cholestyramine, 51224-011 — Cholestyramine, 62135-008 — Cholestyramine for Oral Suspension, 62135-937 — Cholestyramine for Oral Suspension, 63629-2162 — cholestyramine, 63629-2164 — cholestyramine, 63629-9196 — cholestyramine powder for suspension, 63629-9466 — Choleystyramine Light, 67877-298 — cholestyramine powder for suspension, 67877-422 — Choleystyramine Light, 68094-806 — Cholestyramine, 68094-906 — Cholestyramine, 68382-528 — CHOLESTYRAMINE, 68382-529 — CHOLESTYRAMINE, 70771-1105 — CHOLESTYRAMINE, 71335-2902 — cholestyramine powder for suspension, 72162-1504 — cholestyramine, 72162-1505 — cholestyramine, 72162-1834 — cholestyramine powder for suspension, +17 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.