Package 11673-683-80

Brand: ibuprofen mini

Generic: ibuprofen mini 200 mg
NDC Package

Package Facts

Identity

Package NDC 11673-683-80
Digits Only 1167368380
Product NDC 11673-683
Description

1 BOTTLE in 1 CARTON (11673-683-80) / 80 CAPSULE, LIQUID FILLED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2021-12-17
Brand ibuprofen mini
Generic ibuprofen mini 200 mg
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0e082f03-459c-4639-e063-6294a90a6689", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0311673683323", "0311673683668", "0311673683804"], "unii": ["WK2XYI10QM"], "rxcui": ["310964"], "spl_set_id": ["c80426d9-e121-c24d-e053-2a95a90acf2f"], "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": "300 CAPSULE, LIQUID FILLED in 1 BOTTLE (11673-683-32)", "package_ndc": "11673-683-32", "marketing_start_date": "20211217"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (11673-683-66)  / 160 CAPSULE, LIQUID FILLED in 1 BOTTLE", "package_ndc": "11673-683-66", "marketing_start_date": "20211217"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (11673-683-80)  / 80 CAPSULE, LIQUID FILLED in 1 BOTTLE", "package_ndc": "11673-683-80", "marketing_start_date": "20211217"}], "brand_name": "Ibuprofen Mini", "product_id": "11673-683_0e082f03-459c-4639-e063-6294a90a6689", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "11673-683", "generic_name": "Ibuprofen Mini 200 mg", "labeler_name": "TARGET CORPORATION", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ibuprofen Mini", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA079205", "marketing_category": "ANDA", "marketing_start_date": "20211217", "listing_expiration_date": "20261231"}