Package 76420-847-90

Brand: ibuprofen

Generic: ibuprofen
NDC Package

Package Facts

Identity

Package NDC 76420-847-90
Digits Only 7642084790
Product NDC 76420-847
Description

90 TABLET, FILM COATED in 1 BOTTLE (76420-847-90)

Marketing

Marketing Status
Marketed Since 2024-09-08
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": "2195e546-9f39-0130-e063-6294a90ad9c3", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["197805", "197806", "197807"], "spl_set_id": ["ca81671d-1ea8-4c67-802f-adb3a2f087cc"], "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": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (76420-847-01)", "package_ndc": "76420-847-01", "marketing_start_date": "20240908"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (76420-847-05)", "package_ndc": "76420-847-05", "marketing_start_date": "20240908"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (76420-847-30)", "package_ndc": "76420-847-30", "marketing_start_date": "20240908"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (76420-847-60)", "package_ndc": "76420-847-60", "marketing_start_date": "20240908"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (76420-847-90)", "package_ndc": "76420-847-90", "marketing_start_date": "20240908"}], "brand_name": "Ibuprofen", "product_id": "76420-847_2195e546-9f39-0130-e063-6294a90ad9c3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "76420-847", "generic_name": "Ibuprofen", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "600 mg/1"}], "application_number": "ANDA202413", "marketing_category": "ANDA", "marketing_start_date": "20240523", "listing_expiration_date": "20261231"}