Omeprazole Magnesium

Product NDC
0179-8104
11-digit product format
001798104
Labeler code
0179
Product ID
0179-8104_3aed5ccc-4dab-bf13-2ca1-c57f13a09b01
Type
HUMAN OTC DRUG
Nonproprietary name
Omeprazole Magnesium
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Labeler
Kaiser Permanente
Application
ANDA078878
Marketing category
ANDA
Marketing start
2016-01-01
Marketing end
0000-00-00
Substance
OMEPRAZOLE MAGNESIUM
Active strength
20 mg/1
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
0179-8104-42EA - Each0179-8104abc4ff3d-a667-4fbf-ab41-8c2b4053e05112015-09-10

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0179-8104-14001798104141 BOTTLE in 1 CARTON (0179-8104-14) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE1 bottle2016-01-010000-00-00NoNoCurrent
0179-8104-28001798104282 BOTTLE in 1 CARTON (0179-8104-28) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE2 bottle2016-01-010000-00-00NoNoCurrent
0179-8104-42001798104423 BOTTLE in 1 CARTON (0179-8104-42) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE3 bottle2016-01-010000-00-00NoNoCurrent