Package 0363-0368-76

Brand: all day pain relief

Generic: naproxen sodium
NDC Package

Package Facts

Identity

Package NDC 0363-0368-76
Digits Only 0363036876
Product NDC 0363-0368
Description

1 BOTTLE in 1 CARTON (0363-0368-76) / 120 TABLET, FILM COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2002-07-11
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": "889efbbf-10a8-4b8b-b9cb-d8eca7b839c7", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["318d4e2a-7108-4e88-8e56-5bec17ca4a3e"], "manufacturer_name": ["Walgreen Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-0368-71)  / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0363-0368-71", "marketing_start_date": "19970114"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-0368-75)  / 90 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0363-0368-75", "marketing_start_date": "20220726"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-0368-76)  / 120 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0363-0368-76", "marketing_start_date": "20020711"}], "brand_name": "All Day Pain Relief", "product_id": "0363-0368_889efbbf-10a8-4b8b-b9cb-d8eca7b839c7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "0363-0368", "generic_name": "Naproxen Sodium", "labeler_name": "Walgreen Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "All Day Pain Relief", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA074661", "marketing_category": "ANDA", "marketing_start_date": "19970114", "listing_expiration_date": "20261231"}