PRILOSEC

Product NDC
0186-0625
11-digit product format
001860625
Labeler code
0186
Product ID
0186-0625_3209e9cd-92a0-4e3d-8d26-cfb636faff9c
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Omeprazole magnesium
Dosage form
GRANULE, DELAYED RELEASE
Route
ORAL
Labeler
AstraZeneca Pharmaceuticals LP
Application
NDA022056
Marketing category
NDA
Marketing start
2002-02-09
Marketing end
2019-11-01
Substance
OMEPRAZOLE MAGNESIUM
Active strength
3 mg/1
Pharmacologic classes
Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA],Cytochrome P450 2C19 Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0186-0625-01EA - Each0186-06256a84b5fe-59a0-4675-9438-6fe459bc148c12012-07-24