leader omeprazole

Product NDC
37205-837
11-digit product format
372050837
Labeler code
37205
Product ID
37205-837_657afea6-16c2-4dd8-8550-dcd6db03587a
Type
HUMAN OTC DRUG
Nonproprietary name
Omeprazole
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Labeler
Cardinal Health
Application
NDA022032
Marketing category
NDA
Marketing start
2008-02-28
Marketing end
2019-11-01
Substance
OMEPRAZOLE
Active strength
20 mg/1
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
37205-837-06EA - Each37205-8371b3fb889-1d2b-4257-8779-3d9c1d4674fa12012-07-24
37205-837-15EA - Each37205-837e52b6032-9fa0-40e4-90b6-14e70360e3ab12012-07-24
37205-837-66EA - Each37205-8373bc89ad9-78a0-4cf2-be40-8f7340caff8e12013-02-13
37205-837-74EA - Each37205-8379cdcee8e-6515-486c-8ba7-b2be0c437c7b12012-07-24