Package 72789-382-30

Brand: ibuprofen

Generic: ibuprofen
NDC Package

Package Facts

Identity

Package NDC 72789-382-30
Digits Only 7278938230
Product NDC 72789-382
Product ID 72789-382_40bb88fc-9f49-04fa-e063-6294a90a044c
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-382-30)

Marketing

Marketing Status
Marketed Since 2024-02-21
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": "40bb88fc-9f49-04fa-e063-6294a90a044c", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["197807"], "spl_set_id": ["b81c6495-8b30-41ef-8a0f-4cbfd87f1eb4"], "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 (72789-382-30)", "package_ndc": "72789-382-30", "marketing_start_date": "20240221"}], "brand_name": "Ibuprofen", "product_id": "72789-382_40bb88fc-9f49-04fa-e063-6294a90a044c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "72789-382", "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": "ANDA091625", "marketing_category": "ANDA", "marketing_start_date": "20151221", "listing_expiration_date": "20261231"}