Package 72189-318-30

Brand: esomeprazole magnesium

Generic: esomeprazole magnesium
NDC Package

Package Facts

Identity

Package NDC 72189-318-30
Digits Only 7218931830
Product NDC 72189-318
Description

30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72189-318-30)

Marketing

Marketing Status
Marketed Since 2022-01-19
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": "2c3d1a7e-adf4-c587-e063-6394a90a0637", "openfda": {"unii": ["R6DXU4WAY9"], "rxcui": ["606730"], "spl_set_id": ["d5f56bd4-3a59-6857-e053-2995a90a6e00"], "manufacturer_name": ["Direct Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72189-318-30)", "package_ndc": "72189-318-30", "marketing_start_date": "20220119"}], "brand_name": "ESOMEPRAZOLE MAGNESIUM", "product_id": "72189-318_2c3d1a7e-adf4-c587-e063-6394a90a0637", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Cytochrome P450 2C19 Inhibitors [MoA]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "72189-318", "generic_name": "ESOMEPRAZOLE MAGNESIUM", "labeler_name": "Direct Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ESOMEPRAZOLE MAGNESIUM", "active_ingredients": [{"name": "ESOMEPRAZOLE MAGNESIUM", "strength": "40 mg/1"}], "application_number": "ANDA211977", "marketing_category": "ANDA", "marketing_start_date": "20220119", "listing_expiration_date": "20261231"}