0008-0844Level 3
Protonix (PANTOPRAZOLE SODIUM)
**Product type:** Human Prescription Drug
**Active ingredient:** PANTOPRAZOLE SODIUM
**Strength:** 40 mg/1
**Dosage form:** Granule, Delayed Release
**Route:** Oral
**Labeler:** Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
**Marketing category:** NDA (NDA022020)
**Pharmacologic class:** Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
GET
/api/v1/systems/ndc_fda/nodes/0008-0844Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.