Package 70264-011-01

Brand: aleve

Generic: naproxen sodium
NDC Package

Package Facts

Identity

Package NDC 70264-011-01
Digits Only 7026401101
Product NDC 70264-011
Description

50 POUCH in 1 CARTON (70264-011-01) / 1 TABLET in 1 POUCH

Marketing

Marketing Status
Marketed Since 2014-02-26
Brand 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": "43c866a6-dc20-5e19-e063-6294a90aac20", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574", "849728"], "spl_set_id": ["46e7b298-9e19-49b6-be71-e4fdcb09a5d4"], "manufacturer_name": ["R J General Corporation"]}, "finished": true, "packaging": [{"sample": false, "description": "50 POUCH in 1 CARTON (70264-011-01)  / 1 TABLET in 1 POUCH", "package_ndc": "70264-011-01", "marketing_start_date": "20140226"}], "brand_name": "Aleve", "product_id": "70264-011_43c866a6-dc20-5e19-e063-6294a90aac20", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "70264-011", "generic_name": "NAPROXEN SODIUM", "labeler_name": "R J General Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Aleve", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "NDA020204", "marketing_category": "NDA", "marketing_start_date": "20140226", "listing_expiration_date": "20261231"}