Package 70000-0291-1

Brand: ibuprofen

Generic: ibuprofen
NDC Package

Package Facts

Identity

Package NDC 70000-0291-1
Digits Only 7000002911
Product NDC 70000-0291
Description

1 BOTTLE, PLASTIC in 1 CARTON (70000-0291-1) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 1999-03-01
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": "7158f22b-a4bb-445f-8743-7d9feb20d8c4", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0096295131963"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["a41a0bc2-ef7a-44cd-a42e-aefab41323cc"], "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, PLASTIC in 1 CARTON (70000-0291-1)  / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "70000-0291-1", "marketing_start_date": "19990301"}], "brand_name": "Ibuprofen", "product_id": "70000-0291_7158f22b-a4bb-445f-8743-7d9feb20d8c4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "70000-0291", "generic_name": "Ibuprofen", "labeler_name": "Cardinal Health 110, LLC. DBA Leader", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA075139", "marketing_category": "ANDA", "marketing_start_date": "19990301", "listing_expiration_date": "20261231"}