Package 41250-818-62

Brand: naproxen sodium

Generic: naproxen sodium
NDC Package

Package Facts

Identity

Package NDC 41250-818-62
Digits Only 4125081862
Product NDC 41250-818
Description

1 BOTTLE in 1 CARTON (41250-818-62) / 24 TABLET, FILM COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2019-03-26
Brand naproxen sodium
Generic naproxen sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c565e3ca-2202-4806-95a8-1f0e210b6097", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["f4e57560-ae89-4fc3-a66b-ebf3dc3f2448"], "manufacturer_name": ["Meijer Distribution Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (41250-818-62)  / 24 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "41250-818-62", "marketing_start_date": "20190326"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (41250-818-75)  / 90 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "41250-818-75", "marketing_start_date": "20220602"}], "brand_name": "naproxen sodium", "product_id": "41250-818_c565e3ca-2202-4806-95a8-1f0e210b6097", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "41250-818", "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": "20190326", "listing_expiration_date": "20271231"}