Package 41163-050-58

Brand: equaline ibuprofen pm

Generic: diphenhydramine citrate, ibuprofen
NDC Package

Package Facts

Identity

Package NDC 41163-050-58
Digits Only 4116305058
Product NDC 41163-050
Description

1 BOTTLE in 1 CARTON (41163-050-58) / 40 TABLET, FILM COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2009-03-21
Brand equaline 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": "d06f41f5-6ade-4964-a941-d8fc41a39529", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["4OD433S209", "WK2XYI10QM"], "rxcui": ["895664"], "spl_set_id": ["5c4ff82a-bdc4-4df5-9df7-abc6becf4f4d"], "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": ["United Natural Foods, Inc. dba UNFI"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (41163-050-27)  / 80 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "41163-050-27", "marketing_start_date": "20090302"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (41163-050-58)  / 40 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "41163-050-58", "marketing_start_date": "20090321"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (41163-050-60)  / 20 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "41163-050-60", "marketing_start_date": "20120111"}], "brand_name": "equaline ibuprofen pm", "product_id": "41163-050_d06f41f5-6ade-4964-a941-d8fc41a39529", "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": "41163-050", "generic_name": "diphenhydramine citrate, ibuprofen", "labeler_name": "United Natural Foods, Inc. dba UNFI", "product_type": "HUMAN OTC DRUG", "brand_name_base": "equaline 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": "20090302", "listing_expiration_date": "20261231"}