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Colestipol hydrochloride

NDC 70710-1467 · Zydus Pharmaceuticals USA Inc.

Generic nameColestipol hydrochloride
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)COLESTIPOL HYDROCHLORIDE
Strength1 g/1
Pharmacologic classBile Acid Sequestrant [EPC], Bile-acid Binding Activity [MoA]
Marketing categoryANDA

Packages

70710-1467-5 — 500 TABLET, FILM COATED in 1 BOTTLE (70710-1467-5)

70710-1467-7 — 120 TABLET, FILM COATED in 1 BOTTLE (70710-1467-7)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0009-0260 — Colestipol Hydrochloride, 0009-0450 — Colestipol Hydrochloride, 0115-5211 — COLESTIPOL HYDROCHLORIDE, 0115-5212 — COLESTIPOL HYDROCHLORIDE, 0115-5213 — COLESTIPOL HYDROCHLORIDE, 42799-115 — Colestipol Hydrochloride, 50742-284 — Colestipol Hydrochloride, 59762-0260 — Colestipol Hydrochloride, 59762-0450 — Colestipol Hydrochloride, 60687-715 — Colestipol Hydrochloride, 62559-395 — COLESTIPOL HYDROCHLORIDE, 70771-1653 — Colestipol hydrochloride

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

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels