NDC 70518-1829 – Sulfasalazine

Sulfasalazine 500 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70518-1829

Product details

Brand name
Sulfasalazine
Generic name
Sulfasalazine
Labeler
REMEDYREPACK INC.
Dosage form
Tablet
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA007073
Marketed since
January 28, 2019
Listing expires
December 31, 2027
Pharmacologic class
Aminosalicylate

Active ingredients

Uses, dosage, side effects and warnings for Sulfasalazine →

Package NDC codes (1)

Package NDCDescriptionSince
70518-1829-330 TABLET in 1 BLISTER PACK (70518-1829-3)Oct 29, 2021

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