Package 11822-0050-3

Brand: ibuprofen pm

Generic: diphenhydramine citrate, ibuprofen
NDC Package

Package Facts

Identity

Package NDC 11822-0050-3
Digits Only 1182200503
Product NDC 11822-0050
Description

1 BOTTLE in 1 CARTON (11822-0050-3) / 20 TABLET, FILM COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2009-03-19
Brand ibuprofen pm
Generic diphenhydramine citrate, ibuprofen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5f945338-3fd2-4b4d-87e2-2405830dd5f6", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["4OD433S209", "WK2XYI10QM"], "rxcui": ["895664"], "spl_set_id": ["d9eefb84-cc2e-4deb-a1c0-a7c21929f5ac"], "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 (11822-0050-1)  / 80 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "11822-0050-1", "marketing_start_date": "20090624"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (11822-0050-3)  / 20 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "11822-0050-3", "marketing_start_date": "20090319"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (11822-0050-5)  / 120 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "11822-0050-5", "marketing_start_date": "20230823"}], "brand_name": "ibuprofen pm", "product_id": "11822-0050_5f945338-3fd2-4b4d-87e2-2405830dd5f6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "11822-0050", "generic_name": "Diphenhydramine Citrate, Ibuprofen", "labeler_name": "Rite Aid Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ibuprofen pm", "active_ingredients": [{"name": "DIPHENHYDRAMINE CITRATE", "strength": "38 mg/1"}, {"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA079113", "marketing_category": "ANDA", "marketing_start_date": "20090319", "listing_expiration_date": "20261231"}