NDC 0480-7750 – Mesalamine

Mesalamine 800 mg/1 · Tablet, Delayed Release · Oral

Human Prescription Drug

Product NDC0480-7750

Product details

Brand name
Mesalamine
Generic name
Mesalamine
Labeler
Teva Pharmaceuticals, Inc.
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA213191
Marketed since
August 22, 2024
Listing expires
December 31, 2026
Pharmacologic class
Aminosalicylate

Active ingredients

Uses, dosage, side effects and warnings for Mesalamine →

Package NDC codes (1)

Package NDCDescriptionSince
0480-7750-80180 TABLET, DELAYED RELEASE in 1 BOTTLE (0480-7750-80)Aug 22, 2024

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