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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0186-6020-01EA - Each0186-60207999dd36-253f-4e1d-928b-d61675d40b5012012-07-24