Package 68071-3679-1

Brand: ibuprofen

Generic: ibuprofen
NDC Package

Package Facts

Identity

Package NDC 68071-3679-1
Digits Only 6807136791
Product NDC 68071-3679
Description

100 TABLET, FILM COATED in 1 BOTTLE (68071-3679-1)

Marketing

Marketing Status
Marketed Since 2024-09-04
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": "214ded7d-d55c-8b44-e063-6394a90a1a0a", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0368071367911"], "unii": ["WK2XYI10QM"], "rxcui": ["197806"], "spl_set_id": ["214e3b3e-87b9-9ff5-e063-6394a90ae96a"], "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": "100 TABLET, FILM COATED in 1 BOTTLE (68071-3679-1)", "package_ndc": "68071-3679-1", "marketing_start_date": "20240904"}], "brand_name": "Ibuprofen", "product_id": "68071-3679_214ded7d-d55c-8b44-e063-6394a90a1a0a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "68071-3679", "generic_name": "Ibuprofen", "labeler_name": "NuCare Pharmaceuticals, 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"}