Esomeprazole Sodium
- Product NDC
- 55150-184
- 11-digit product format
- 551500184
- Labeler code
- 55150
- Product ID
- 55150-184_6aeefceb-9bbc-4e7a-8b30-a0c338ca89f4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Esomeprazole Sodium
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- AuroMedics Pharma LLC
- Application
- ANDA204657
- Marketing category
- ANDA
- Marketing start
- 2016-08-10
- Marketing end
- 0000-00-00
- Substance
- ESOMEPRAZOLE SODIUM
- Active strength
- 20 mg/1
- 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