Package 11822-6604-2
Brand: ibuprofen
Generic: ibuprofenPackage Facts
Identity
Package NDC
11822-6604-2
Digits Only
1182266042
Product NDC
11822-6604
Description
1 BOTTLE in 1 CARTON (11822-6604-2) / 50 TABLET, FILM COATED in 1 BOTTLE
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": "2ceba01b-fad3-4aca-8df7-84bc6372c96e", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["1dba3cb7-2e3d-4378-93cf-92db8f24f41f"], "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": ["Rite Aid Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (11822-6604-2) / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "11822-6604-2", "marketing_end_date": "20270228", "marketing_start_date": "20230410"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (11822-6604-3) / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "11822-6604-3", "marketing_end_date": "20261031", "marketing_start_date": "20230410"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (11822-6604-4)", "package_ndc": "11822-6604-4", "marketing_end_date": "20270228", "marketing_start_date": "20230410"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (11822-6604-5) / 24 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "11822-6604-5", "marketing_end_date": "20260930", "marketing_start_date": "20221109"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (11822-6604-6) / 200 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "11822-6604-6", "marketing_end_date": "20260930", "marketing_start_date": "20221109"}], "brand_name": "Ibuprofen", "product_id": "11822-6604_2ceba01b-fad3-4aca-8df7-84bc6372c96e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "11822-6604", "generic_name": "Ibuprofen", "labeler_name": "Rite Aid Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA072096", "marketing_category": "ANDA", "marketing_end_date": "20270228", "marketing_start_date": "20200904"}