Omeprazole

Product NDC
50090-7472
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Omeprazole
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA078490
Marketing category
ANDA
Substance
OMEPRAZOLE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-7472-030 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7472-0) 2024-12-12NoHistorical
50090-7472-215 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7472-2) 2024-12-12NoHistorical
50090-7472-360 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7472-3) 2024-12-12NoHistorical
50090-7472-420 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7472-4) 2024-12-12NoHistorical
50090-7472-590 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7472-5) 2024-12-12NoHistorical
50090-7472-6200 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7472-6) 2024-12-12NoHistorical
50090-7472-7180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7472-7) 2024-12-12NoHistorical
50090-7472-87 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7472-8) 2024-12-12NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
OmeprazoleA-S Medication Solutions2024-12-16HUMAN PRESCRIPTION DRUG LABEL1