Package 47682-488-50

Brand: bayer aleve

Generic: naproxen sodium
NDC Package

Package Facts

Identity

Package NDC 47682-488-50
Digits Only 4768248850
Product NDC 47682-488
Description

50 POUCH in 1 BOX (47682-488-50) / 1 TABLET in 1 POUCH

Marketing

Marketing Status
Marketed Since 2014-01-24
Brand bayer aleve
Generic naproxen sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3e5d43d6-74c5-08f6-e063-6394a90a0a54", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574", "849728"], "spl_set_id": ["5dd569ca-d03e-410c-af98-4732c823d595"], "manufacturer_name": ["Unifirst First Aid Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 POUCH in 1 BOX (47682-488-50)  / 1 TABLET in 1 POUCH", "package_ndc": "47682-488-50", "marketing_start_date": "20140124"}], "brand_name": "Bayer Aleve", "product_id": "47682-488_3e5d43d6-74c5-08f6-e063-6394a90a0a54", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "47682-488", "generic_name": "Naproxen Sodium", "labeler_name": "Unifirst First Aid Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Bayer Aleve", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "NDA020204", "marketing_category": "NDA", "marketing_start_date": "20140124", "listing_expiration_date": "20261231"}