NDC 0013-0101 – Azulfidine

Sulfasalazine 500 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC0013-0101

Product details

Brand name
Azulfidine
Generic name
Sulfasalazine
Labeler
Pfizer Laboratories Div Pfizer Inc
Dosage form
Tablet
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
0013-0101-101 BOTTLE in 1 CARTON (0013-0101-10) / 100 TABLET in 1 BOTTLEFeb 27, 2020
0013-0101-301 BOTTLE in 1 CARTON (0013-0101-30) / 300 TABLET in 1 BOTTLEFeb 27, 2020

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