Package 11822-0084-6

Brand: ibuprofen and pseudoephedrine hydrochloride

Generic: ibuprofen and pseudoephedrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 11822-0084-6
Digits Only 1182200846
Product NDC 11822-0084
Description

1 BLISTER PACK in 1 CARTON (11822-0084-6) / 40 TABLET, COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2018-02-01
Brand ibuprofen and pseudoephedrine hydrochloride
Generic ibuprofen and pseudoephedrine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "61dd37ef-591d-42c8-9bdc-bd2a6073e63b", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM", "6V9V2RYJ8N"], "rxcui": ["1299021"], "spl_set_id": ["483c3bb7-529e-4684-80e1-6646b050988e"], "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"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (11822-0084-5)  / 20 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "11822-0084-5", "marketing_start_date": "20180201"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (11822-0084-6)  / 40 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "11822-0084-6", "marketing_start_date": "20180201"}], "brand_name": "Ibuprofen and Pseudoephedrine Hydrochloride", "product_id": "11822-0084_61dd37ef-591d-42c8-9bdc-bd2a6073e63b", "dosage_form": "TABLET, COATED", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "11822-0084", "generic_name": "Ibuprofen and Pseudoephedrine Hydrochloride", "labeler_name": "Rite-Aid", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ibuprofen and Pseudoephedrine Hydrochloride", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}, {"name": "PSEUDOEPHEDRINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA074567", "marketing_category": "ANDA", "marketing_start_date": "20180201", "listing_expiration_date": "20261231"}