Package 50844-261-08

Brand: naproxen

Generic: naproxen sodium
NDC Package

Package Facts

Identity

Package NDC 50844-261-08
Digits Only 5084426108
Product NDC 50844-261
Description

1 BOTTLE, PLASTIC in 1 CARTON (50844-261-08) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2019-08-06
Brand naproxen
Generic naproxen sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f5f6ef48-fa2a-4a62-9cde-0a685fe575b0", "openfda": {"upc": ["0052548689827"], "unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["82412133-c11a-4905-a119-965f44de10b7"], "manufacturer_name": ["L.N.K. International, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (50844-261-08)  / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "50844-261-08", "marketing_start_date": "20190806"}], "brand_name": "Naproxen", "product_id": "50844-261_f5f6ef48-fa2a-4a62-9cde-0a685fe575b0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "50844-261", "generic_name": "Naproxen Sodium", "labeler_name": "L.N.K. International, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naproxen", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA204872", "marketing_category": "ANDA", "marketing_start_date": "20190806", "listing_expiration_date": "20261231"}