NDC 68382-711 – Mesalamine

Mesalamine 1.2 g/1 · Tablet, Delayed Release · Oral

Human Prescription Drug

Product NDC68382-711

Product details

Brand name
Mesalamine
Generic name
Mesalamine
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA091640
Marketed since
June 19, 2017
Listing expires
December 31, 2026
Pharmacologic class
Aminosalicylate

Active ingredients

Uses, dosage, side effects and warnings for Mesalamine →

Package NDC codes (2)

Package NDCDescriptionSince
68382-711-19120 TABLET, DELAYED RELEASE in 1 BOTTLE (68382-711-19)Jun 19, 2017
68382-711-6434 TABLET, DELAYED RELEASE in 1 BOTTLE (68382-711-64)Jun 19, 2017

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