Package 59779-647-71

Brand: ibuprofen

Generic: ibuprofen
NDC Package

Package Facts

Identity

Package NDC 59779-647-71
Digits Only 5977964771
Product NDC 59779-647
Description

1 BOTTLE in 1 CARTON (59779-647-71) / 50 TABLET, FILM COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2001-07-31
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": "86c7adc3-20a1-4477-91a4-9804feba6220", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["e655bd64-dd82-46d8-87cc-2674beaffe20"], "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": ["CVS Pharmacy"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (59779-647-71)  / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "59779-647-71", "marketing_start_date": "20010731"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (59779-647-78)  / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "59779-647-78", "marketing_start_date": "20010802"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (59779-647-90)", "package_ndc": "59779-647-90", "marketing_start_date": "20070328"}, {"sample": false, "description": "2 BOTTLE in 1 PACKAGE (59779-647-93)  / 500 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "59779-647-93", "marketing_start_date": "20250610"}], "brand_name": "ibuprofen", "product_id": "59779-647_86c7adc3-20a1-4477-91a4-9804feba6220", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "59779-647", "generic_name": "Ibuprofen", "labeler_name": "CVS Pharmacy", "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": "20010731", "listing_expiration_date": "20261231"}