Package 79903-389-50

Brand: all day pain relief

Generic: naproxen sodium
NDC Package

Package Facts

Identity

Package NDC 79903-389-50
Digits Only 7990338950
Product NDC 79903-389
Description

1 BOTTLE in 1 CARTON (79903-389-50) / 50 TABLET in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2025-05-10
Brand all day pain relief
Generic naproxen sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "34ae94cb-6d62-c8f2-e063-6394a90aa297", "openfda": {"upc": ["0194346497980"], "unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["32df7378-4dd1-4f7e-e063-6394a90ad948"], "manufacturer_name": ["Walmart Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (79903-389-50)  / 50 TABLET in 1 BOTTLE", "package_ndc": "79903-389-50", "marketing_start_date": "20250510"}], "brand_name": "All Day Pain Relief", "product_id": "79903-389_34ae94cb-6d62-c8f2-e063-6394a90aa297", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "79903-389", "generic_name": "Naproxen Sodium", "labeler_name": "Walmart Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "All Day Pain Relief", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA090545", "marketing_category": "ANDA", "marketing_start_date": "20250510", "listing_expiration_date": "20261231"}