esomeprazole magnesium

Generic: esomeprazole magnesium

Labeler: retail business services, llc.
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name esomeprazole magnesium
Generic Name esomeprazole magnesium
Labeler retail business services, llc.
Dosage Form CAPSULE, DELAYED RELEASE
Routes
ORAL
Active Ingredients

esomeprazole magnesium dihydrate 20 mg/1

Manufacturer
Retail Business Services, LLC.

Identifiers & Regulatory

Product NDC 72476-500
Product ID 72476-500_855f7fd6-0c28-4eea-8c9d-466d79782133
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA209339
Listing Expiration 2026-12-31
Marketing Start 2017-10-16

Pharmacologic Class

Classes
cytochrome p450 2c19 inhibitors [moa] proton pump inhibitor [epc] proton pump inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72476500
Hyphenated Format 72476-500

Supplemental Identifiers

RxCUI
606726
UNII
36H71644EQ

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name esomeprazole magnesium (source: ndc)
Generic Name esomeprazole magnesium (source: ndc)
Application Number ANDA209339 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 3 BOTTLE in 1 CARTON (72476-500-03) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (72476-500-05) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE
source: ndc

Packages (2)

72476-500-03 3 BOTTLE in 1 CARTON (72476-500-03) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE 72476-500-05 1 BOTTLE in 1 CARTON (72476-500-05) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE

Ingredients (1)

esomeprazole magnesium dihydrate (20 mg/1)

Linked Drug Pages (1)

Esomeprazole Magnesium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "855f7fd6-0c28-4eea-8c9d-466d79782133", "openfda": {"unii": ["36H71644EQ"], "rxcui": ["606726"], "spl_set_id": ["ce376d91-0ea8-4922-9f7f-707420cb1d96"], "manufacturer_name": ["Retail Business Services, LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BOTTLE in 1 CARTON (72476-500-03)  / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE", "package_ndc": "72476-500-03", "marketing_start_date": "20171016"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (72476-500-05)  / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE", "package_ndc": "72476-500-05", "marketing_start_date": "20171016"}], "brand_name": "Esomeprazole Magnesium", "product_id": "72476-500_855f7fd6-0c28-4eea-8c9d-466d79782133", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Cytochrome P450 2C19 Inhibitors [MoA]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "72476-500", "generic_name": "Esomeprazole Magnesium", "labeler_name": "Retail Business Services, LLC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Esomeprazole Magnesium", "active_ingredients": [{"name": "ESOMEPRAZOLE MAGNESIUM DIHYDRATE", "strength": "20 mg/1"}], "application_number": "ANDA209339", "marketing_category": "ANDA", "marketing_start_date": "20171016", "listing_expiration_date": "20261231"}