esomeprazole magnesium

Generic: esomeprazole magnesium

Labeler: aurohealth llc
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name esomeprazole magnesium
Generic Name esomeprazole magnesium
Labeler aurohealth llc
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

esomeprazole magnesium dihydrate 20 mg/1

Manufacturer
Aurohealth LLC

Identifiers & Regulatory

Product NDC 58602-840
Product ID 58602-840_5ddd44f1-1baa-4730-b718-5d1c326ecd49
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA214473
Listing Expiration 2027-12-31
Marketing Start 2023-07-12

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 58602840
Hyphenated Format 58602-840

Supplemental Identifiers

RxCUI
433733
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 ANDA214473 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (58602-840-05) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
  • 2 BOTTLE in 1 CARTON (58602-840-61) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
  • 3 BOTTLE in 1 CARTON (58602-840-62) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
source: ndc

Packages (3)

58602-840-05 1 BOTTLE in 1 CARTON (58602-840-05) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE 58602-840-61 2 BOTTLE in 1 CARTON (58602-840-61) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE 58602-840-62 3 BOTTLE in 1 CARTON (58602-840-62) / 14 TABLET, 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": "5ddd44f1-1baa-4730-b718-5d1c326ecd49", "openfda": {"unii": ["36H71644EQ"], "rxcui": ["433733"], "spl_set_id": ["034bcbad-f57f-4338-a193-7a5aa9f09aa6"], "manufacturer_name": ["Aurohealth LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-840-05)  / 14 TABLET, DELAYED RELEASE in 1 BOTTLE", "package_ndc": "58602-840-05", "marketing_start_date": "20230712"}, {"sample": false, "description": "2 BOTTLE in 1 CARTON (58602-840-61)  / 14 TABLET, DELAYED RELEASE in 1 BOTTLE", "package_ndc": "58602-840-61", "marketing_start_date": "20230712"}, {"sample": false, "description": "3 BOTTLE in 1 CARTON (58602-840-62)  / 14 TABLET, DELAYED RELEASE in 1 BOTTLE", "package_ndc": "58602-840-62", "marketing_start_date": "20230712"}], "brand_name": "Esomeprazole Magnesium", "product_id": "58602-840_5ddd44f1-1baa-4730-b718-5d1c326ecd49", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Cytochrome P450 2C19 Inhibitors [MoA]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "58602-840", "generic_name": "Esomeprazole Magnesium", "labeler_name": "Aurohealth LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Esomeprazole Magnesium", "active_ingredients": [{"name": "ESOMEPRAZOLE MAGNESIUM DIHYDRATE", "strength": "20 mg/1"}], "application_number": "ANDA214473", "marketing_category": "ANDA", "marketing_start_date": "20230712", "listing_expiration_date": "20271231"}