Basic Care Omeprazole

Product NDC
0113-7915
11-digit product format
001137915
Labeler code
0113
Product ID
0113-7915_3f8dd174-2e24-40b6-ae02-41061abe609e
Type
HUMAN OTC DRUG
Nonproprietary name
Omeprazole
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Labeler
L. Perrigo Company
Application
NDA022032
Marketing category
NDA
Marketing start
2017-08-08
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
0113-7915-01001137915011 BOTTLE in 1 CARTON (0113-7915-01) > 14 TABLET, DELAYED RELEASE in 1 BOTTLE1 bottle2017-08-100000-00-00NoNoCurrent
0113-7915-30001137915302 CARTON in 1 CARTON (0113-7915-30) > 14 BLISTER PACK in 1 CARTON > 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK2 carton2018-10-080000-00-00NoNoCurrent
0113-7915-55001137915553 CARTON in 1 CARTON (0113-7915-55) > 14 BLISTER PACK in 1 CARTON > 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK3 carton2017-08-080000-00-00NoNoCurrent