Acid Reducer

Product NDC
37808-856
11-digit product format
378080856
Labeler code
37808
Product ID
37808-856_785cc2f6-6621-4870-8b38-3525dbb3b84a
Type
HUMAN OTC DRUG
Nonproprietary name
Esomeprazole magnesium
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Labeler
H E B
Application
ANDA212088
Marketing category
ANDA
Marketing start
2022-03-31
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 Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37808-856ACID REDUCER (ESOMEPRAZOLE MAGNESIUM) TABLET, DELAYED RELEASE [H E B]3Legacy NDC20250306_f55c896a-0906-4245-bcc4-8cd851163f0b.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
37808-856-14378080856141 BOTTLE, PLASTIC in 1 CARTON (37808-856-14) > 14 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC2022-03-310000-00-00NoNoCurrent
37808-856-42378080856423 BOTTLE, PLASTIC in 1 CARTON (37808-856-42) > 14 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC2022-03-310000-00-00NoNoCurrent