Acid Reducer

Product NDC
11822-5600
11-digit product format
118225600
Labeler code
11822
Product ID
11822-5600_2385e2e4-e70b-4aca-9db8-905fe4cd3971
Type
HUMAN OTC DRUG
Nonproprietary name
Esomeprazole magnesium
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Labeler
Rite Aid Corporation
Application
ANDA212088
Marketing category
ANDA
Marketing start
2021-07-23
Marketing end
0000-00-00
Substance
ESOMEPRAZOLE MAGNESIUM
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
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d7006a36-e68d-42e2-8cd3-d725cb2e47b1Product name620251027
d71865e8-5c35-4d76-8ecd-a7adda982240Product name920180628
d71865e8-5c35-4d76-8ecd-a7adda982240Product name820171212
094c6751-235c-4d12-acee-2baf94f676f4Product name120151116
ce67e27d-1d21-5465-4409-b0662dd99d4dProduct name120140508

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11822-5600ACID REDUCER (ESOMEPRAZOLE MAGNESIUM) TABLET, DELAYED RELEASE [RITE AID CORPORATION]6Legacy NDC20240216_94b3c883-6d6c-4fa8-8430-7f979e6d2a97.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
11822-5600-2118225600023 BOTTLE in 1 CARTON (11822-5600-2) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE3 bottle2021-07-230000-00-00NoNoCurrent
11822-5600-4118225600043 BOTTLE, PLASTIC in 1 CARTON (11822-5600-4) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC2021-07-230000-00-00NoNoCurrent