Package 70000-0731-1

Brand: esomeprazole magnesium

Generic: esomeprazole magnesium
NDC Package

Package Facts

Identity

Package NDC 70000-0731-1
Digits Only 7000007311
Product NDC 70000-0731
Description

2 BOTTLE in 1 CARTON (70000-0731-1) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70000-0731-2)

Marketing

Marketing Status
Marketed Since 2025-04-09
Brand esomeprazole magnesium
Generic esomeprazole magnesium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3fad3e71-9b6c-4b72-8637-2ac587b5861a", "openfda": {"unii": ["36H71644EQ"], "rxcui": ["606726"], "spl_set_id": ["c98b4332-ce47-422e-be54-f3eee0762354"], "manufacturer_name": ["LEADER/ CARDINAL HEALTH 110, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BOTTLE in 1 CARTON (70000-0731-1)  / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70000-0731-2)", "package_ndc": "70000-0731-1", "marketing_start_date": "20250409"}], "brand_name": "ESOMEPRAZOLE MAGNESIUM", "product_id": "70000-0731_3fad3e71-9b6c-4b72-8637-2ac587b5861a", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Cytochrome P450 2C19 Inhibitors [MoA]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "70000-0731", "generic_name": "ESOMEPRAZOLE MAGNESIUM", "labeler_name": "LEADER/ CARDINAL HEALTH 110, INC.", "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": "20250409", "listing_expiration_date": "20261231"}