Package 63941-245-03

Brand: all day pain relief

Generic: naproxen sodium
NDC Package

Package Facts

Identity

Package NDC 63941-245-03
Digits Only 6394124503
Product NDC 63941-245
Product ID 63941-245_28729f2d-cd7e-c174-e063-6394a90ac876
Description

1 BOTTLE, PLASTIC in 1 CARTON (63941-245-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Discontinued 2027-09-30
Brand all day pain relief
Generic naproxen sodium
Sample Package No

Linked Drug Pages (1)

All Day Pain Relief ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "28729f2d-cd7e-c174-e063-6394a90ac876", "openfda": {"upc": ["0070038577805"], "unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["593b915f-045a-40b7-b86e-0d1cb41f2bb8"], "manufacturer_name": ["VALU MERCHANDISERS COMPANY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (63941-245-01)  / 24 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "63941-245-01", "marketing_end_date": "20261130", "marketing_start_date": "20100610"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (63941-245-02)  / 50 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "63941-245-02", "marketing_end_date": "20261130", "marketing_start_date": "20100519"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (63941-245-03)  / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "63941-245-03", "marketing_end_date": "20270930", "marketing_start_date": "20100519"}], "brand_name": "All Day Pain Relief", "product_id": "63941-245_28729f2d-cd7e-c174-e063-6394a90ac876", "dosage_form": "TABLET, COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "63941-245", "generic_name": "NAPROXEN SODIUM", "labeler_name": "VALU MERCHANDISERS COMPANY", "product_type": "HUMAN OTC DRUG", "brand_name_base": "All Day Pain Relief", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA079096", "marketing_category": "ANDA", "marketing_end_date": "20270930", "marketing_start_date": "20100519"}