Package 41250-477-71

Brand: naproxen sodium

Generic: naproxen sodium
NDC Package

Package Facts

Identity

Package NDC 41250-477-71
Digits Only 4125047771
Product NDC 41250-477
Product ID 41250-477_05bd2fec-f777-4753-b864-b3d406fb0678
Description

1 BOTTLE in 1 CARTON (41250-477-71) / 50 TABLET, FILM COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2014-03-05
Brand naproxen sodium
Generic naproxen sodium
Sample Package No

Linked Drug Pages (1)

Naproxen Sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "05bd2fec-f777-4753-b864-b3d406fb0678", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["9551e84b-19bc-43e7-9c6e-0f24fdeb5abe"], "manufacturer_name": ["Meijer Distribution Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (41250-477-62)  / 24 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "41250-477-62", "marketing_start_date": "20180706"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (41250-477-71)  / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "41250-477-71", "marketing_start_date": "20140305"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (41250-477-75)  / 90 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "41250-477-75", "marketing_start_date": "20220526"}, {"sample": false, "description": "400 TABLET, FILM COATED in 1 BOTTLE (41250-477-79)", "package_ndc": "41250-477-79", "marketing_start_date": "20140305"}], "brand_name": "Naproxen Sodium", "product_id": "41250-477_05bd2fec-f777-4753-b864-b3d406fb0678", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "41250-477", "generic_name": "Naproxen Sodium", "labeler_name": "Meijer Distribution Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naproxen Sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA074661", "marketing_category": "ANDA", "marketing_start_date": "20140305", "listing_expiration_date": "20261231"}