Package 79903-609-09

Brand: all day back and muscle pain relief

Generic: naproxen sodium
NDC Package

Package Facts

Identity

Package NDC 79903-609-09
Digits Only 7990360909
Product NDC 79903-609
Product ID 79903-609_0bafa4ac-8c2d-006b-e063-6294a90ab1fc
Description

1 BOTTLE in 1 CARTON (79903-609-09) / 90 TABLET, COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2023-12-15
Brand all day back and muscle pain relief
Generic naproxen sodium
Sample Package No

Linked Drug Pages (1)

All Day Back and Muscle Pain Relief ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0bafa4ac-8c2d-006b-e063-6294a90ab1fc", "openfda": {"upc": ["0194346189106", "0194346189113"], "unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["062b9ffe-b4fc-9f5a-e063-6294a90a560e"], "manufacturer_name": ["Walmart Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (79903-609-09)  / 90 TABLET, COATED in 1 BOTTLE", "package_ndc": "79903-609-09", "marketing_start_date": "20231215"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (79903-609-20)  / 200 TABLET, COATED in 1 BOTTLE", "package_ndc": "79903-609-20", "marketing_start_date": "20231215"}], "brand_name": "All Day Back and Muscle Pain Relief", "product_id": "79903-609_0bafa4ac-8c2d-006b-e063-6294a90ab1fc", "dosage_form": "TABLET, COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "79903-609", "generic_name": "Naproxen sodium", "labeler_name": "Walmart Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "All Day Back and Muscle Pain Relief", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA090545", "marketing_category": "ANDA", "marketing_start_date": "20231215", "listing_expiration_date": "20261231"}