NDC 62756-238 – Capecitabine

Capecitabine 150 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC62756-238

Product details

Brand name
Capecitabine
Generic name
Capecitabine
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA204668
Marketed since
September 1, 2019
Listing expires
December 31, 2026
Pharmacologic class
Nucleoside Metabolic Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Capecitabine →

Package NDC codes (3)

Package NDCDescriptionSince
62756-238-181000 TABLET, FILM COATED in 1 BOTTLE (62756-238-18)Sep 1, 2019
62756-238-8660 TABLET, FILM COATED in 1 BOTTLE (62756-238-86)Sep 1, 2019
62756-238-88100 TABLET, FILM COATED in 1 BOTTLE (62756-238-88)Sep 1, 2019

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