Package 72789-543-14

Brand: naproxen sodium

Generic: naproxen sodium
NDC Package

Package Facts

Identity

Package NDC 72789-543-14
Digits Only 7278954314
Product NDC 72789-543
Product ID 72789-543_46b3a114-167a-d337-e063-6394a90a9a33
Description

14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-543-14)

Marketing

Marketing Status
Marketed Since 2025-12-23
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": "46b3a114-167a-d337-e063-6394a90a9a33", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["d2b1eedb-2be0-42af-ba0b-9da98560c91e"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-543-14)", "package_ndc": "72789-543-14", "marketing_start_date": "20251223"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-543-28)", "package_ndc": "72789-543-28", "marketing_start_date": "20251223"}], "brand_name": "Naproxen Sodium", "product_id": "72789-543_46b3a114-167a-d337-e063-6394a90a9a33", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "72789-543", "generic_name": "Naproxen Sodium", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naproxen Sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA074661", "marketing_category": "ANDA", "marketing_start_date": "20140411", "listing_expiration_date": "20261231"}