Esomeprazole Magnesium

Product NDC
30142-528
11-digit product format
301420528
Labeler code
30142
Product ID
30142-528_10d3d4ce-4256-3df7-9d73-813bf8aa924e
Type
HUMAN OTC DRUG
Nonproprietary name
Esomeprazole Magnesium
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Labeler
KROGER COMPANY
Application
ANDA207198
Marketing category
ANDA
Marketing start
2025-03-01
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
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
R6DXU4WAY9ESOMEPRAZOLE MAGNESIUM217087-09-7ESOMEPRAZOLE MAGNESIUM

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
30142-528-14301420528141 BOTTLE in 1 CARTON (30142-528-14) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE1 bottle2025-03-01NoNoHistorical
30142-528-42301420528423 BOTTLE in 1 CARTON (30142-528-42) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE3 bottle2025-03-01NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Drug FactsKROGER COMPANY2025-10-28HUMAN OTC DRUG LABEL2
Drug FactsKROGER COMPANY2024-07-29HUMAN OTC DRUG LABEL1