Lansoprazole

Product NDC
11822-0016
11-digit product format
118220016
Labeler code
11822
Product ID
11822-0016_2ccb0862-4c9a-ee5e-9ccd-257c0c88e6f4
Type
HUMAN OTC DRUG
Nonproprietary name
Lansoprazole
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Labeler
Rite Aid Corporation
Application
ANDA202194
Marketing category
ANDA
Marketing start
2022-09-01
Marketing end
0000-00-00
Substance
LANSOPRAZOLE
Active strength
15 mg/1
Pharmacologic classes
Inhibition Gastric Acid Secretion [PE], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11822-0016LANSOPRAZOLE CAPSULE, DELAYED RELEASE [RITE AID CORPORATION]2Legacy NDC20231103_049c2673-587d-8e3c-207d-9a63108bf159.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
11822-0016-1118220016011 BOTTLE in 1 CARTON (11822-0016-1) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE1 bottle2022-09-010000-00-00NoNoCurrent
11822-0016-3118220016033 BOTTLE in 1 CARTON (11822-0016-3) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE3 bottle2022-09-010000-00-00NoNoCurrent