Package 51655-275-21

Brand: ibuprofen

Generic: ibuprofen
NDC Package

Package Facts

Identity

Package NDC 51655-275-21
Digits Only 5165527521
Product NDC 51655-275
Description

21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-275-21)

Marketing

Marketing Status
Marketed Since 2020-10-29
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": "48e6db4e-3114-e1b6-e063-6294a90a281e", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["197807"], "spl_set_id": ["c20f1f4d-59b3-6bbe-e053-2a95a90abaf1"], "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 (51655-275-20)", "package_ndc": "51655-275-20", "marketing_start_date": "20210709"}, {"sample": false, "description": "21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-275-21)", "package_ndc": "51655-275-21", "marketing_start_date": "20201029"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-275-25)", "package_ndc": "51655-275-25", "marketing_start_date": "20210217"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-275-26)", "package_ndc": "51655-275-26", "marketing_start_date": "20200616"}, {"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-275-54)", "package_ndc": "51655-275-54", "marketing_start_date": "20200921"}], "brand_name": "Ibuprofen", "product_id": "51655-275_48e6db4e-3114-e1b6-e063-6294a90a281e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "51655-275", "generic_name": "Ibuprofen", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "800 mg/1"}], "application_number": "ANDA090796", "marketing_category": "ANDA", "marketing_start_date": "20200616", "listing_expiration_date": "20271231"}