Package 72789-391-90

Brand: esomeprazole magnesium

Generic: esomeprazole magnesium
NDC Package

Package Facts

Identity

Package NDC 72789-391-90
Digits Only 7278939190
Product NDC 72789-391
Description

90 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-391-90)

Marketing

Marketing Status
Marketed Since 2024-04-09
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": "412329bd-ce50-d48d-e063-6294a90a9399", "openfda": {"upc": ["0372789391908"], "unii": ["R6DXU4WAY9"], "rxcui": ["606730"], "spl_set_id": ["fdea1f5f-b717-4d49-8d70-0b373c959bf0"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-391-90)", "package_ndc": "72789-391-90", "marketing_start_date": "20240409"}], "brand_name": "Esomeprazole Magnesium", "product_id": "72789-391_412329bd-ce50-d48d-e063-6294a90a9399", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Cytochrome P450 2C19 Inhibitors [MoA]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "72789-391", "generic_name": "Esomeprazole Magnesium", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Esomeprazole Magnesium", "active_ingredients": [{"name": "ESOMEPRAZOLE MAGNESIUM", "strength": "40 mg/1"}], "application_number": "ANDA078279", "marketing_category": "ANDA", "marketing_start_date": "20151210", "listing_expiration_date": "20261231"}