Package 24979-254-06

Brand: naproxen sodium

Generic: naproxen sodium
NDC Package

Package Facts

Identity

Package NDC 24979-254-06
Digits Only 2497925406
Product NDC 24979-254
Product ID 24979-254_a79a3bf0-fe2f-4ba4-8eaa-e1c97ab9b927
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (24979-254-06)

Marketing

Marketing Status
Marketed Since 2024-04-25
Brand naproxen sodium
Generic naproxen sodium
Sample Package No

Linked Drug Pages (1)

Naproxen Sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "a79a3bf0-fe2f-4ba4-8eaa-e1c97ab9b927", "openfda": {"upc": ["0324979252018", "0324979254067", "0324979253688"], "unii": ["9TN87S3A3C"], "rxcui": ["1116320", "1116339", "1116349"], "spl_set_id": ["7c22a2d6-821c-4f83-aead-e756aed930e5"], "manufacturer_name": ["Upsher-Smith Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (24979-254-06)", "package_ndc": "24979-254-06", "marketing_start_date": "20240425"}], "brand_name": "Naproxen Sodium", "product_id": "24979-254_a79a3bf0-fe2f-4ba4-8eaa-e1c97ab9b927", "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": "24979-254", "generic_name": "Naproxen Sodium", "labeler_name": "Upsher-Smith Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naproxen Sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "750 mg/1"}], "application_number": "NDA020353", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20240425", "listing_expiration_date": "20261231"}