NDC 68382-435 – Mesalamine

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

Human Prescription Drug

Product NDC68382-435

Product details

Brand name
Mesalamine
Generic name
Mesalamine
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA203286
Marketed since
August 2, 2018
Listing expires
December 31, 2027
Pharmacologic class
Aminosalicylate

Active ingredients

Uses, dosage, side effects and warnings for Mesalamine →

Package NDC codes (2)

Package NDCDescriptionSince
68382-435-28180 TABLET, DELAYED RELEASE in 1 BOTTLE (68382-435-28)Aug 2, 2018
68382-435-7710 BLISTER PACK in 1 CARTON (68382-435-77) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (68382-435-30)Aug 2, 2018

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