Package 70000-0176-5

Brand: leader ibuprofen

Generic: ibuprofen
NDC Package

Package Facts

Identity

Package NDC 70000-0176-5
Digits Only 7000001765
Product NDC 70000-0176
Description

1 BOTTLE in 1 CARTON (70000-0176-5) / 500 TABLET, FILM COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2017-05-04
Brand leader ibuprofen
Generic ibuprofen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ead9d7b1-1a6b-4b01-9c26-35b457c93eac", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["63b8d389-7feb-41d2-8970-b7d5660ccb4a"], "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": ["Cardinal Health 110, LLC. dba Leader"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (70000-0176-1)  / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "70000-0176-1", "marketing_start_date": "20161130"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (70000-0176-4)  / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "70000-0176-4", "marketing_start_date": "20170504"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (70000-0176-5)  / 500 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "70000-0176-5", "marketing_start_date": "20170504"}], "brand_name": "Leader Ibuprofen", "product_id": "70000-0176_ead9d7b1-1a6b-4b01-9c26-35b457c93eac", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "70000-0176", "generic_name": "Ibuprofen", "labeler_name": "Cardinal Health 110, LLC. dba Leader", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Leader Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA072096", "marketing_category": "ANDA", "marketing_start_date": "20161130", "listing_expiration_date": "20261231"}