OMEPRAZOLE

Product NDC
71335-1627
11-digit product format
713351627
Labeler code
71335
Product ID
71335-1627_f177e371-dee5-4924-90ad-8e142b4a2a49
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Omeprazole
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA091672
Marketing category
ANDA
Marketing start
2014-10-31
Marketing end
0000-00-00
Substance
OMEPRAZOLE
Active strength
20 mg/1
Pharmacologic classes
Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA],Cytochrome P450 2C19 Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
71335-1627-0713351627007 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1627-0) 2014-10-310000-00-00NoNoCurrent
71335-1627-17133516270130 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1627-1) 2014-10-310000-00-00NoNoCurrent
71335-1627-27133516270260 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1627-2) 2014-10-310000-00-00NoNoCurrent
71335-1627-37133516270356 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1627-3) 2014-10-310000-00-00NoNoCurrent
71335-1627-47133516270490 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1627-4) 2014-10-310000-00-00NoNoCurrent
71335-1627-57133516270520 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1627-5) 2014-10-310000-00-00NoNoCurrent
71335-1627-67133516270615 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1627-6) 2014-10-310000-00-00NoNoCurrent
71335-1627-771335162707120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1627-7) 2014-10-310000-00-00NoNoCurrent
71335-1627-871335162708100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1627-8) 2014-10-310000-00-00NoNoCurrent
71335-1627-97133516270928 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1627-9) 2014-10-310000-00-00NoNoCurrent