Package 50844-353-02

Brand: ibuprofen

Generic: ibuprofen
NDC Package

Package Facts

Identity

Package NDC 50844-353-02
Digits Only 5084435302
Product NDC 50844-353
Description

1 BOTTLE, PLASTIC in 1 CARTON (50844-353-02) / 12 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": "5f8c5841-a57f-4394-bbc2-93fc48474282", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0050844353169"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["c93da67f-f42e-4baa-976b-73c71ba6dd71"], "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": ["L.N.K. International, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (50844-353-02)  / 12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "50844-353-02", "marketing_start_date": "19990301"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-353-16)", "package_ndc": "50844-353-16", "marketing_start_date": "19990301"}], "brand_name": "Ibuprofen", "product_id": "50844-353_5f8c5841-a57f-4394-bbc2-93fc48474282", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "50844-353", "generic_name": "ibuprofen", "labeler_name": "L.N.K. International, Inc.", "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": "20271231"}