Package 72789-389-60

Brand: naproxen sodium

Generic: naproxen sodium
NDC Package

Package Facts

Identity

Package NDC 72789-389-60
Digits Only 7278938960
Product NDC 72789-389
Description

60 TABLET in 1 BOTTLE, PLASTIC (72789-389-60)

Marketing

Marketing Status
Marketed Since 2024-04-01
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": "47a9b7b5-2b1d-7a8e-e063-6294a90a1f63", "openfda": {"upc": ["0372789389608"], "unii": ["9TN87S3A3C"], "rxcui": ["849431"], "spl_set_id": ["145cdcc0-9bd5-4a0e-81fc-11a24d181980"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (72789-389-60)", "package_ndc": "72789-389-60", "marketing_start_date": "20240401"}], "brand_name": "Naproxen Sodium", "product_id": "72789-389_47a9b7b5-2b1d-7a8e-e063-6294a90a1f63", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "72789-389", "generic_name": "Naproxen Sodium", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naproxen Sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "550 mg/1"}], "application_number": "ANDA212199", "marketing_category": "ANDA", "marketing_start_date": "20191030", "listing_expiration_date": "20271231"}