NDC 72603-817 – Colestipol Hydrochloride

Colestipol Hydrochloride 1 g/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC72603-817

Product details

Brand name
Colestipol Hydrochloride
Generic name
Colestipol Hydrochloride
Labeler
NorthStar Rx LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA216517
Marketed since
September 1, 2026
Listing expires
December 31, 2027
Pharmacologic class
Bile Acid Sequestrant

Active ingredients

Uses, dosage, side effects and warnings for Colestipol Hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
72603-817-01120 TABLET, FILM COATED in 1 BOTTLE (72603-817-01)Sep 1, 2026

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