Package 68071-5126-3
Brand: ibuprofen
Generic: ibuprofenPackage Facts
Identity
Package NDC
68071-5126-3
Digits Only
6807151263
Product NDC
68071-5126
Description
30 TABLET, FILM COATED in 1 BOTTLE (68071-5126-3)
Marketing
Marketing Status
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": "1b549eac-763d-ab7a-e063-6294a90a72f7", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0368071512694"], "unii": ["WK2XYI10QM"], "rxcui": ["197805"], "spl_set_id": ["9973bfa2-693a-1165-e053-2995a90a4b1d"], "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": "30 TABLET, FILM COATED in 1 BOTTLE (68071-5126-3)", "package_ndc": "68071-5126-3", "marketing_start_date": "20191211"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68071-5126-9)", "package_ndc": "68071-5126-9", "marketing_start_date": "20191211"}], "brand_name": "IBUPROFEN", "product_id": "68071-5126_1b549eac-763d-ab7a-e063-6294a90a72f7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "68071-5126", "generic_name": "IBUPROFEN", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "IBUPROFEN", "active_ingredients": [{"name": "IBUPROFEN", "strength": "400 mg/1"}], "application_number": "ANDA090796", "marketing_category": "ANDA", "marketing_start_date": "20151230", "listing_expiration_date": "20261231"}