Package 71205-787-00

Brand: ibuprofen

Generic: ibuprofen
NDC Package

Package Facts

Identity

Package NDC 71205-787-00
Digits Only 7120578700
Product NDC 71205-787
Description

100 TABLET, FILM COATED in 1 BOTTLE (71205-787-00)

Marketing

Marketing Status
Marketed Since 2023-04-06
Brand ibuprofen
Generic ibuprofen
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4ee828df-873d-4379-9a17-a805d97dfe04", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0371205787004"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["4ee828df-873d-4379-9a17-a805d97dfe04"], "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": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71205-787-00)", "package_ndc": "71205-787-00", "marketing_start_date": "20230406"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-787-30)", "package_ndc": "71205-787-30", "marketing_start_date": "20230406"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-787-60)", "package_ndc": "71205-787-60", "marketing_start_date": "20230406"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-787-90)", "package_ndc": "71205-787-90", "marketing_start_date": "20230406"}], "brand_name": "ibuprofen", "product_id": "71205-787_4ee828df-873d-4379-9a17-a805d97dfe04", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "71205-787", "generic_name": "Ibuprofen", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA072096", "marketing_category": "ANDA", "marketing_start_date": "19940816", "listing_expiration_date": "20261231"}