Package 85509-1203-1

Brand: naproxen and esomeprazole magnesium

Generic: naproxen and esomeprazole magnesium
NDC Package

Package Facts

Identity

Package NDC 85509-1203-1
Digits Only 8550912031
Product NDC 85509-1203
Description

60 TABLET, DELAYED RELEASE in 1 BOTTLE (85509-1203-1)

Marketing

Marketing Status
Marketed Since 2025-08-01
Brand naproxen and esomeprazole magnesium
Generic naproxen and esomeprazole magnesium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3c550f7b-3a41-f64f-e063-6394a90ab3a9", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["R6DXU4WAY9", "57Y76R9ATQ"], "rxcui": ["994008"], "spl_set_id": ["3a652450-525b-4839-e063-6294a90ac287"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]"], "pharm_class_epc": ["Nonsteroidal Anti-inflammatory Drug [EPC]"], "pharm_class_moa": ["Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["PHOENIX RX LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (85509-1203-1)", "package_ndc": "85509-1203-1", "marketing_start_date": "20250801"}, {"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (85509-1203-3)", "package_ndc": "85509-1203-3", "marketing_start_date": "20250721"}], "brand_name": "Naproxen and esomeprazole magnesium", "product_id": "85509-1203_3c550f7b-3a41-f64f-e063-6394a90ab3a9", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Cytochrome P450 2C19 Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "85509-1203", "generic_name": "Naproxen and esomeprazole magnesium", "labeler_name": "PHOENIX RX LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naproxen and esomeprazole magnesium", "active_ingredients": [{"name": "ESOMEPRAZOLE MAGNESIUM", "strength": "20 mg/1"}, {"name": "NAPROXEN", "strength": "500 mg/1"}], "application_number": "ANDA213699", "marketing_category": "ANDA", "marketing_start_date": "20221006", "listing_expiration_date": "20261231"}