Package 69420-1375-1
Brand: naproxen sodium
Generic: naproxen sodiumPackage 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
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"}