Package 0363-0291-29
Brand: ibuprofen
Generic: ibuprofenPackage Facts
Identity
Package NDC
0363-0291-29
Digits Only
0363029129
Product NDC
0363-0291
Description
150 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0363-0291-29)
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": "93d5e52b-b346-422b-b801-25ce2a20888b", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["c118b290-f821-4e73-906e-8a93edaf34e4"], "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": ["Walgreen Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0363-0291-03)", "package_ndc": "0363-0291-03", "marketing_start_date": "19880524"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0363-0291-14)", "package_ndc": "0363-0291-14", "marketing_start_date": "19980524"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0363-0291-16)", "package_ndc": "0363-0291-16", "marketing_start_date": "20230525"}, {"sample": false, "description": "150 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0363-0291-29)", "package_ndc": "0363-0291-29", "marketing_start_date": "19880524"}], "brand_name": "Ibuprofen", "product_id": "0363-0291_93d5e52b-b346-422b-b801-25ce2a20888b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "0363-0291", "generic_name": "Ibuprofen", "labeler_name": "Walgreen Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA075010", "marketing_category": "ANDA", "marketing_start_date": "19880524", "listing_expiration_date": "20261231"}