Package 11673-050-58

Brand: up and up ibuprofen pm

Generic: diphenhydramine citrate and ibuprofen
NDC Package

Package Facts

Identity

Package NDC 11673-050-58
Digits Only 1167305058
Product NDC 11673-050
Description

1 BOTTLE in 1 CARTON (11673-050-58) / 40 TABLET, FILM COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2009-07-24
Brand up and up ibuprofen pm
Generic diphenhydramine citrate and ibuprofen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7533fd37-bf20-484b-8030-c1cd2f6eaa0e", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["4OD433S209", "WK2XYI10QM"], "rxcui": ["895664"], "spl_set_id": ["0c764683-f3c9-4382-96be-d34b7a582aee"], "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": "1 BOTTLE in 1 CARTON (11673-050-58)  / 40 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "11673-050-58", "marketing_start_date": "20090724"}, {"sample": false, "description": "200 TABLET, FILM COATED in 1 BOTTLE (11673-050-82)", "package_ndc": "11673-050-82", "marketing_start_date": "20220127"}], "brand_name": "up and up ibuprofen pm", "product_id": "11673-050_7533fd37-bf20-484b-8030-c1cd2f6eaa0e", "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": "11673-050", "generic_name": "diphenhydramine citrate and ibuprofen", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "up and up 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": "20090710", "listing_expiration_date": "20261231"}