NDC 70771-1653 – Colestipol hydrochloride

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

Human Prescription Drug

Product NDC70771-1653

Product details

Brand name
Colestipol hydrochloride
Generic name
Colestipol hydrochloride
Labeler
Zydus Lifesciences Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA215223
Marketed since
May 4, 2022
Listing expires
December 31, 2026
Pharmacologic class
Bile Acid Sequestrant

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
70771-1653-5500 TABLET, FILM COATED in 1 BOTTLE (70771-1653-5)May 4, 2022
70771-1653-7120 TABLET, FILM COATED in 1 BOTTLE (70771-1653-7)May 4, 2022

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