Package 72789-218-30

Brand: ibuprofen

Generic: ibuprofen
NDC Package

Package Facts

Identity

Package NDC 72789-218-30
Digits Only 7278921830
Product NDC 72789-218
Product ID 72789-218_341840c3-856e-5d1f-e063-6394a90a9d0a
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-218-30)

Marketing

Marketing Status
Marketed Since 2025-10-09
Brand ibuprofen
Generic ibuprofen
Sample Package No

Linked Drug Pages (1)

Ibuprofen ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "341840c3-856e-5d1f-e063-6394a90a9d0a", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0372789218304"], "unii": ["WK2XYI10QM"], "rxcui": ["197807"], "spl_set_id": ["7942cc53-1268-4e5f-8db0-f0b3524bb744"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]"], "pharm_class_epc": ["Nonsteroidal Anti-inflammatory Drug [EPC]"], "pharm_class_moa": ["Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-218-30)", "package_ndc": "72789-218-30", "marketing_start_date": "20251009"}], "brand_name": "Ibuprofen", "product_id": "72789-218_341840c3-856e-5d1f-e063-6394a90a9d0a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "72789-218", "generic_name": "Ibuprofen", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "800 mg/1"}], "application_number": "ANDA078329", "marketing_category": "ANDA", "marketing_start_date": "20200821", "listing_expiration_date": "20261231"}