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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50436-3121-1EA - Each50436-31218d72a276-59d0-4973-ada6-f3c059e0439812015-10-02