Omeprazole

Product NDC
60760-489
11-digit product format
607600489
Labeler code
60760
Product ID
60760-489_f19ddbec-d77c-a3f1-e053-2a95a90a65d5
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
omeprazole
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Labeler
St. Mary's Medical Park Pharmacy
Application
ANDA075410
Marketing category
ANDA
Marketing start
2021-05-21
Marketing end
0000-00-00
Substance
OMEPRAZOLE
Active strength
20 mg/1
Pharmacologic classes
Cytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2024-12-31
Current FDA listing
Historical FDA.report record

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60760-489OMEPRAZOLE CAPSULE, DELAYED RELEASE [ST. MARY'S MEDICAL PARK PHARMACY]2Legacy NDC20230112_c32d1a5d-bfbd-9604-e053-2995a90a49c5.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
60760-489-07607600489077 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-489-07) 2021-06-070000-00-00NoNoCurrent
60760-489-306076004893030 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-489-30) 2021-05-210000-00-00NoNoCurrent
60760-489-606076004896060 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-489-60) 2021-06-070000-00-00NoNoCurrent
60760-489-906076004899090 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-489-90) 2021-05-210000-00-00NoNoCurrent