NDC 71610-706 – Sulfasalazine

Sulfasalazine 500 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71610-706

Product details

Brand name
Sulfasalazine
Generic name
Sulfasalazine
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Tablet
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA007073
Marketed since
July 1, 2003
Listing expires
December 31, 2026
Pharmacologic class
Aminosalicylate

Active ingredients

Uses, dosage, side effects and warnings for Sulfasalazine →

Package NDC codes (2)

Package NDCDescriptionSince
71610-706-70120 TABLET in 1 BOTTLE (71610-706-70)May 16, 2023
71610-706-80180 TABLET in 1 BOTTLE (71610-706-80)May 16, 2023

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