NDC 0013-0102 – Azulfidine EN-tabs

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

Human Prescription Drug

Product NDC0013-0102

Product details

Brand name
Azulfidine EN-tabs
Generic name
Sulfasalazine
Labeler
Pfizer Laboratories Div Pfizer Inc
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
NDA · NDA007073
Marketed since
June 20, 1950
Listing expires
December 31, 2027
Pharmacologic class
Aminosalicylate

Active ingredients

Uses, dosage, side effects and warnings for Azulfidine →

Package NDC codes (2)

Package NDCDescriptionSince
0013-0102-501 BOTTLE in 1 CARTON (0013-0102-50) / 100 TABLET, DELAYED RELEASE in 1 BOTTLEJul 7, 2020
0013-0102-601 BOTTLE in 1 CARTON (0013-0102-60) / 300 TABLET, DELAYED RELEASE in 1 BOTTLEFeb 15, 2021

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