Package 45802-490-75

Brand: naproxen sodium

Generic: naproxen sodium
NDC Package

Package Facts

Identity

Package NDC 45802-490-75
Digits Only 4580249075
Product NDC 45802-490
Description

1 BOTTLE in 1 CARTON (45802-490-75) / 90 TABLET, FILM COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2021-12-02
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": "d92cd99a-ffdc-41e9-a7c3-8447910c3b92", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["cdb60f74-ce23-4015-90eb-b23a2275f6cb"], "manufacturer_name": ["Padagis Israel Pharmaceuticals Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (45802-490-75)  / 90 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "45802-490-75", "marketing_start_date": "20211202"}], "brand_name": "Naproxen Sodium", "product_id": "45802-490_d92cd99a-ffdc-41e9-a7c3-8447910c3b92", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "45802-490", "generic_name": "Naproxen Sodium", "labeler_name": "Padagis Israel Pharmaceuticals Ltd", "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": "20140411", "listing_expiration_date": "20271231"}