Package 72789-187-30

Brand: ibuprofen

Generic: ibuprofen
NDC Package

Package Facts

Identity

Package NDC 72789-187-30
Digits Only 7278918730
Product NDC 72789-187
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-187-30)

Marketing

Marketing Status
Marketed Since 2021-05-18
Brand ibuprofen
Generic ibuprofen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "34178401-0edc-512f-e063-6294a90ab88a", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0372789186825", "0372789187822", "0372789185309"], "unii": ["WK2XYI10QM"], "rxcui": ["197805", "197806", "197807"], "spl_set_id": ["3732defa-67c2-4b84-8a84-4bbc27b6cb24"], "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 (72789-187-30)", "package_ndc": "72789-187-30", "marketing_start_date": "20210518"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-187-60)", "package_ndc": "72789-187-60", "marketing_start_date": "20200821"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-187-82)", "package_ndc": "72789-187-82", "marketing_start_date": "20210518"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-187-90)", "package_ndc": "72789-187-90", "marketing_start_date": "20210518"}], "brand_name": "Ibuprofen", "product_id": "72789-187_34178401-0edc-512f-e063-6294a90ab88a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "72789-187", "generic_name": "Ibuprofen", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "600 mg/1"}], "application_number": "ANDA078329", "marketing_category": "ANDA", "marketing_start_date": "20200821", "listing_expiration_date": "20261231"}