Package 80425-0384-1
Brand: ibuprofen and famotidine
Generic: ibuprofen and famotidinePackage Facts
Identity
Package NDC
80425-0384-1
Digits Only
8042503841
Product NDC
80425-0384
Description
30 TABLET in 1 BOTTLE (80425-0384-1)
Marketing
Marketing Status
Brand
ibuprofen and famotidine
Generic
ibuprofen and famotidine
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "16c8a378-4a4c-885f-e063-6394a90acd4b", "openfda": {"nui": ["N0000000151", "N0000175784", "N0000000160", "M0001335", "N0000175722"], "unii": ["5QZO15J2Z8", "WK2XYI10QM"], "rxcui": ["1100066"], "spl_set_id": ["16c8b0db-37d0-99d9-e063-6394a90ac31b"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]", "Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["Advanced Rx Pharmacy of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (80425-0384-1)", "package_ndc": "80425-0384-1", "marketing_start_date": "20240423"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (80425-0384-2)", "package_ndc": "80425-0384-2", "marketing_start_date": "20240423"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (80425-0384-3)", "package_ndc": "80425-0384-3", "marketing_start_date": "20240423"}], "brand_name": "IBUPROFEN AND FAMOTIDINE", "product_id": "80425-0384_16c8a378-4a4c-885f-e063-6394a90acd4b", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "80425-0384", "generic_name": "Ibuprofen and famotidine", "labeler_name": "Advanced Rx Pharmacy of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "IBUPROFEN AND FAMOTIDINE", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "26.6 mg/1"}, {"name": "IBUPROFEN", "strength": "800 mg/1"}], "application_number": "ANDA216814", "marketing_category": "ANDA", "marketing_start_date": "20240423", "listing_expiration_date": "20261231"}