Package 0480-0953-56

Brand: naproxen sodium

Generic: naproxen sodium
NDC Package

Package Facts

Identity

Package NDC 0480-0953-56
Digits Only 0480095356
Product NDC 0480-0953
Product ID 0480-0953_6d02cbbb-bfb4-4c68-8a7b-4207f6f9cfbb
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0480-0953-56)

Marketing

Marketing Status
Marketed Since 2022-11-01
Brand naproxen sodium
Generic naproxen sodium
Sample Package No

Linked Drug Pages (1)

Naproxen Sodium, Naproxen sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "6d02cbbb-bfb4-4c68-8a7b-4207f6f9cfbb", "openfda": {"upc": ["0304800953567", "0304800952584", "0304800951013"], "unii": ["9TN87S3A3C"], "rxcui": ["1116320", "1116339", "1116349"], "spl_set_id": ["826fd9e3-22fe-408b-820c-f2b710189555"], "manufacturer_name": ["Teva Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0480-0953-56)", "package_ndc": "0480-0953-56", "marketing_start_date": "20221101"}], "brand_name": "Naproxen Sodium", "product_id": "0480-0953_6d02cbbb-bfb4-4c68-8a7b-4207f6f9cfbb", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "0480-0953", "generic_name": "naproxen sodium", "labeler_name": "Teva Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naproxen Sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "750 mg/1"}], "application_number": "ANDA075416", "marketing_category": "ANDA", "marketing_start_date": "20221101", "listing_expiration_date": "20261231"}