Omeprazole

Product NDC
37012-915
11-digit product format
370120915
Labeler code
37012
Product ID
37012-915_e2370e53-57c3-4a9a-890f-04f8b8922e38
Type
HUMAN OTC DRUG
Nonproprietary name
Omeprazole
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Labeler
Shopko Stores Operating Co., LLC
Application
NDA022032
Marketing category
NDA
Marketing start
2013-06-05
Marketing end
0000-00-00
Substance
OMEPRAZOLE
Active strength
20 mg/1
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
37012-915-03370120915033 BOTTLE in 1 CARTON (37012-915-03) > 14 TABLET, DELAYED RELEASE in 1 BOTTLE3 bottle2015-03-040000-00-00NoNoCurrent
37012-915-30370120915302 CARTON in 1 CARTON (37012-915-30) > 14 BLISTER PACK in 1 CARTON > 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK2 carton2013-06-100000-00-00NoNoCurrent
37012-915-55370120915553 CARTON in 1 CARTON (37012-915-55) > 14 BLISTER PACK in 1 CARTON > 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK3 carton2013-06-130000-00-00NoNoCurrent
37012-915-743701209157414 BLISTER PACK in 1 CARTON (37012-915-74) > 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK14 blister pack2013-06-050000-00-00NoNoCurrent