NDC 11534-201 – Sulfasalazine
Sulfasalazine 500 mg/1 · Tablet, Delayed Release · Oral
Product NDC11534-201
Product details
- Brand name
- Sulfasalazine
- Generic name
- Sulfasalazine
- Labeler
- Sunrise Pharmaceutical, Inc.
- Dosage form
- Tablet, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA075339
- Marketed since
- December 11, 2025
- Listing expires
- December 31, 2026
- Pharmacologic class
- Aminosalicylate
Active ingredients
- Sulfasalazine 500 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 11534-201-01 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE (11534-201-01) | Dec 11, 2025 |
| 11534-201-07 | 300 TABLET, DELAYED RELEASE in 1 BOTTLE (11534-201-07) | Dec 11, 2025 |
Other Sulfasalazine products
- 59762-0104 Sulfasalazine 500 mg/1 · Tablet, Delayed Release · Mylan Pharmaceuticals Inc.
- 50090-0086 Sulfasalazine 500 mg/1 · Tablet · A-S Medication Solutions
- 50090-6936 Sulfasalazine 500 mg/1 · Tablet · A-S Medication Solutions
- 71610-706 Sulfasalazine 500 mg/1 · Tablet · Aphena Pharma Solutions - Tennessee, LLC
- 63629-9715 Sulfasalazine 500 mg/1 · Tablet · Bryant Ranch Prepack
- 62135-960 Sulfasalazine 500 mg/1 · Tablet · Chartwell RX, LLC.
- 59762-5000 Sulfasalazine 500 mg/1 · Tablet · Mylan Pharmaceuticals Inc.
- 70518-1829 Sulfasalazine 500 mg/1 · Tablet · REMEDYREPACK INC.
- 16571-261 Sulfasalazine 500 mg/1 · Tablet · Rising Pharma Holdings, Inc.
- 11534-200 Sulfasalazine 500 mg/1 · Tablet · Sunrise Pharmaceutical, Inc.
- 0093-3234 Sulfasalazine 500 mg/1 · Tablet · Teva Pharmaceuticals USA, Inc.