Package 11673-991-20

Brand: ibuprofen

Generic: ibuprofen
NDC Package

Package Facts

Identity

Package NDC 11673-991-20
Digits Only 1167399120
Product NDC 11673-991
Description

200 TABLET, COATED in 1 BOTTLE (11673-991-20)

Marketing

Marketing Status
Marketed Since 2020-02-04
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": "0e071c42-0f7e-586e-e063-6394a90a9533", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0349483601886", "0349483601206", "0349483991505"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["8e86ae68-7687-79d6-e053-2995a90ac274"], "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": ["TARGET CORPORATION"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (11673-991-01)", "package_ndc": "11673-991-01", "marketing_start_date": "20200204"}, {"sample": false, "description": "50 TABLET, COATED in 1 BOTTLE (11673-991-05)", "package_ndc": "11673-991-05", "marketing_start_date": "20200204"}, {"sample": false, "description": "200 TABLET, COATED in 1 BOTTLE (11673-991-20)", "package_ndc": "11673-991-20", "marketing_start_date": "20200204"}, {"sample": false, "description": "500 TABLET, COATED in 1 BOTTLE (11673-991-50)", "package_ndc": "11673-991-50", "marketing_start_date": "20200204"}, {"sample": false, "description": "1000 TABLET, COATED in 1 BOTTLE (11673-991-88)", "package_ndc": "11673-991-88", "marketing_start_date": "20200204"}], "brand_name": "IBUPROFEN", "product_id": "11673-991_0e071c42-0f7e-586e-e063-6394a90a9533", "dosage_form": "TABLET, COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "11673-991", "generic_name": "IBUPROFEN", "labeler_name": "TARGET CORPORATION", "product_type": "HUMAN OTC DRUG", "brand_name_base": "IBUPROFEN", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA091239", "marketing_category": "ANDA", "marketing_start_date": "20200204", "listing_expiration_date": "20261231"}