NDC 59762-0104 – Sulfasalazine

Sulfasalazine 500 mg/1 · Tablet, Delayed Release · Oral

Human Prescription Drug

Product NDC59762-0104

Product details

Brand name
Sulfasalazine
Generic name
Sulfasalazine
Labeler
Mylan Pharmaceuticals Inc.
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA007073
Marketed since
May 5, 2005
Listing expires
December 31, 2027
Pharmacologic class
Aminosalicylate

Active ingredients

Uses, dosage, side effects and warnings for Sulfasalazine →

Package NDC codes (2)

Package NDCDescriptionSince
59762-0104-51 BOTTLE in 1 CARTON (59762-0104-5) / 100 TABLET, DELAYED RELEASE in 1 BOTTLEMar 23, 2020
59762-0104-61 BOTTLE in 1 CARTON (59762-0104-6) / 300 TABLET, DELAYED RELEASE in 1 BOTTLEApr 6, 2020

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