NDC 0093-3234 – Sulfasalazine

Sulfasalazine 500 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC0093-3234

Product details

Brand name
Sulfasalazine
Generic name
Sulfasalazine
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA085828
Marketed since
December 15, 2022
Listing expires
December 31, 2026
Pharmacologic class
Aminosalicylate

Active ingredients

Uses, dosage, side effects and warnings for Sulfasalazine →

Package NDC codes (3)

Package NDCDescriptionSince
0093-3234-01100 TABLET in 1 BOTTLE, PLASTIC (0093-3234-01)Dec 15, 2022
0093-3234-05500 TABLET in 1 BOTTLE, PLASTIC (0093-3234-05)Feb 27, 2023
0093-3234-101000 TABLET in 1 BOTTLE, PLASTIC (0093-3234-10)Dec 15, 2022

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