11534-201Level 3
Sulfasalazine (Sulfasalazine)
**Product type:** Human Prescription Drug
**Active ingredient:** SULFASALAZINE
**Strength:** 500 mg/1
**Dosage form:** Tablet, Delayed Release
**Route:** Oral
**Labeler:** Sunrise Pharmaceutical, Inc.
**Marketing category:** ANDA (ANDA075339)
**Pharmacologic class:** Aminosalicylate [EPC], Aminosalicylic Acids [CS]
GET
/api/v1/systems/ndc_fda/nodes/11534-201Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.