Package 50090-0685-1

Brand: naproxen sodium

Generic: naproxen sodium
NDC Package

Package Facts

Identity

Package NDC 50090-0685-1
Digits Only 5009006851
Product NDC 50090-0685
Product ID 50090-0685_d4d91910-46d3-43d1-b15a-f3b511ff3b45
Description

10 TABLET, FILM COATED in 1 BOTTLE (50090-0685-1)

Marketing

Marketing Status
Marketed Since 2018-10-31
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": "d4d91910-46d3-43d1-b15a-f3b511ff3b45", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["2523a4de-1af9-46f4-93dc-e8b4029d69c4"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (50090-0685-1)", "package_ndc": "50090-0685-1", "marketing_start_date": "20181031"}], "brand_name": "Naproxen Sodium", "product_id": "50090-0685_d4d91910-46d3-43d1-b15a-f3b511ff3b45", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "50090-0685", "generic_name": "Naproxen Sodium", "labeler_name": "A-S Medication Solutions", "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": "20261231"}