OMEPRAZOLE

Product NDC
71205-959
11-digit product format
712050959
Labeler code
71205
Product ID
71205-959_703a7b68-480c-4f73-9f29-ba86ce95eab3
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
OMEPRAZOLE
Dosage form
CAPSULE, DELAYED RELEASE PELLETS
Route
ORAL
Labeler
Proficient Rx LP
Application
ANDA203481
Marketing category
ANDA
Marketing start
2017-07-03
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

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71205-959OMEPRAZOLE CAPSULE, DELAYED RELEASE PELLETS [PROFICIENT RX LP]1Legacy NDC20200807_703a7b68-480c-4f73-9f29-ba86ce95eab3.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
71205-959-0071205095900100 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71205-959-00) 2020-08-060000-00-00NoNoCurrent
71205-959-11712050959111000 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71205-959-11) 2020-08-060000-00-00NoNoCurrent
71205-959-307120509593030 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71205-959-30) 2020-08-060000-00-00NoNoCurrent
71205-959-5571205095955500 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71205-959-55) 2020-08-060000-00-00NoNoCurrent
71205-959-607120509596060 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71205-959-60) 2020-08-060000-00-00NoNoCurrent
71205-959-907120509599090 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71205-959-90) 2020-08-060000-00-00NoNoCurrent