NEXIUM
- Product NDC
- 50436-3121
- 11-digit product format
- 504363121
- Labeler code
- 50436
- Product ID
- 50436-3121_5e637840-e5e7-4b81-8837-5d2fde2be7f8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Esomeprazole magnesium
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- NDA021153
- Marketing category
- NDA
- Marketing start
- 2001-03-19
- Marketing end
- 0000-00-00
- Substance
- ESOMEPRAZOLE MAGNESIUM
- Active strength
- 40 mg/1
- Pharmacologic classes
- Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA],Cytochrome P450 2C19 Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record