Package 51655-474-26
Brand: ibuprofen
Generic: ibuprofenPackage Facts
Identity
Package NDC
51655-474-26
Digits Only
5165547426
Product NDC
51655-474
Description
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-474-26)
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": "490f163b-b179-d74b-e063-6394a90ad438", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["197806"], "spl_set_id": ["dac07d8f-6b6f-20ab-e053-2a95a90af3ba"], "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": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-474-20)", "package_ndc": "51655-474-20", "marketing_start_date": "20201119"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-474-25)", "package_ndc": "51655-474-25", "marketing_start_date": "20201113"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-474-26)", "package_ndc": "51655-474-26", "marketing_start_date": "20220621"}, {"sample": false, "description": "40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-474-51)", "package_ndc": "51655-474-51", "marketing_start_date": "20210208"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-474-52)", "package_ndc": "51655-474-52", "marketing_start_date": "20210114"}], "brand_name": "Ibuprofen", "product_id": "51655-474_490f163b-b179-d74b-e063-6394a90ad438", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "51655-474", "generic_name": "Ibuprofen", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "600 mg/1"}], "application_number": "ANDA090796", "marketing_category": "ANDA", "marketing_start_date": "20201113", "listing_expiration_date": "20271231"}