Package 69420-1375-1

Brand: naproxen sodium

Generic: naproxen sodium
NDC Package

Package Facts

Identity

Package NDC 69420-1375-1
Digits Only 6942013751
Product NDC 69420-1375
Description

100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69420-1375-1)

Marketing

Marketing Status
Marketed Since 2019-05-01
Brand naproxen sodium
Generic naproxen sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f34d9d85-4a82-43b6-bf5b-3b2893c6b009", "openfda": {"upc": ["0369420137513"], "unii": ["9TN87S3A3C"], "rxcui": ["1116320"], "spl_set_id": ["313dd447-4b9f-4e5b-8ca9-4a2a5a1a53d9"], "manufacturer_name": ["SA3, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69420-1375-1)", "package_ndc": "69420-1375-1", "marketing_start_date": "20190501"}], "brand_name": "Naproxen Sodium", "product_id": "69420-1375_f34d9d85-4a82-43b6-bf5b-3b2893c6b009", "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": "69420-1375", "generic_name": "Naproxen Sodium", "labeler_name": "SA3, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naproxen Sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "375 mg/1"}], "application_number": "NDA020353", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20190501", "listing_expiration_date": "20261231"}