Package 79903-098-06

Brand: All Day Back and Muscle Pain Relief

Generic: Naproxen Sodium
NDC Package

Package Facts

Identity

Package NDC 79903-098-06
Digits Only 7990309806
Product NDC 79903-098
Description

1 BOTTLE, PLASTIC in 1 CARTON (79903-098-06) / 200 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Discontinued 2026-02-28
Brand All Day Back and Muscle 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": "92579484-1eab-438a-8079-984015a1dd9f", "openfda": {"upc": ["0681131071307"], "unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["b54250d5-edcc-450a-9b87-d7bdb5fc301b"], "manufacturer_name": ["WALMART INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (79903-098-06)  / 200 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "79903-098-06", "marketing_end_date": "20260228", "marketing_start_date": "20220117"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (79903-098-52)  / 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "79903-098-52", "marketing_end_date": "20260228", "marketing_start_date": "20220117"}], "brand_name": "All Day Back and Muscle Pain Relief", "product_id": "79903-098_92579484-1eab-438a-8079-984015a1dd9f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "79903-098", "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": "ANDA204872", "marketing_category": "ANDA", "marketing_end_date": "20260228", "marketing_start_date": "20220117"}