NEXIUM
- Product NDC
- 0186-6020
- 11-digit product format
- 001866020
- Labeler code
- 0186
- Product ID
- 0186-6020_abff7986-83f6-4d9f-a322-a6037796b0c1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Esomeprazole sodium
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- AstraZeneca Pharmaceuticals LP
- Application
- NDA021689
- Marketing category
- NDA
- Marketing start
- 2005-05-03
- Marketing end
- 0000-00-00
- Substance
- ESOMEPRAZOLE SODIUM
- Active strength
- 20 mg/5mL
- Pharmacologic classes
- Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA],Cytochrome P450 2C19 Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record