70954-797Level 3
Omeprazole and Sodium Bicarbonate (Omeprazole and Sodium Bicarbonate)
**Product type:** Human Prescription Drug
**Active ingredient:** OMEPRAZOLE; SODIUM BICARBONATE
**Strength:** 20; 1680 mg/1; mg/1
**Dosage form:** Powder, For Suspension
**Route:** Oral
**Labeler:** ANI Pharmaceuticals, Inc.
**Marketing category:** ANDA (ANDA219161)
**Pharmacologic class:** Alkalinizing Activity [MoA], Cytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
GET
/api/v1/systems/ndc_fda/nodes/70954-797Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.