Package 68071-3793-1

Brand: ibuprofen

Generic: ibuprofen
NDC Package

Package Facts

Identity

Package NDC 68071-3793-1
Digits Only 6807137931
Product NDC 68071-3793
Description

21 TABLET, FILM COATED in 1 BOTTLE (68071-3793-1)

Marketing

Marketing Status
Marketed Since 2025-04-07
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": "32376f92-2ad2-7676-e063-6394a90adf0c", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0368071379334"], "unii": ["WK2XYI10QM"], "rxcui": ["197807"], "spl_set_id": ["2e0f74a5-b8f3-fc81-e063-6394a90a647a"], "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": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "21 TABLET, FILM COATED in 1 BOTTLE (68071-3793-1)", "package_ndc": "68071-3793-1", "marketing_start_date": "20250407"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68071-3793-3)", "package_ndc": "68071-3793-3", "marketing_start_date": "20250213"}, {"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (68071-3793-5)", "package_ndc": "68071-3793-5", "marketing_start_date": "20250311"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68071-3793-6)", "package_ndc": "68071-3793-6", "marketing_start_date": "20250213"}], "brand_name": "Ibuprofen", "product_id": "68071-3793_32376f92-2ad2-7676-e063-6394a90adf0c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "68071-3793", "generic_name": "Ibuprofen", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "800 mg/1"}], "application_number": "ANDA202413", "marketing_category": "ANDA", "marketing_start_date": "20240523", "listing_expiration_date": "20261231"}