Package 0067-8205-01

Brand: theraflu flu relief max strength nighttime

Generic: acetaminophen, chlorpheniramine maleate, dextromethorphan hbr
NDC Package

Package Facts

Identity

Package NDC 0067-8205-01
Digits Only 0067820501
Product NDC 0067-8205
Product ID 0067-8205_446e5d67-95c9-e039-e063-6294a90a6cfa
Description

245.5 mL in 1 BOTTLE (0067-8205-01)

Marketing

Marketing Status
Marketed Since 2022-06-27
Brand theraflu flu relief max strength nighttime
Generic acetaminophen, chlorpheniramine maleate, dextromethorphan hbr
Sample Package No

Linked Drug Pages (1)

Theraflu Flu Relief Max Strength Nighttime ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "446e5d67-95c9-e039-e063-6294a90a6cfa", "openfda": {"unii": ["362O9ITL9D", "V1Q0O9OJ9Z", "9D2RTI9KYH"], "rxcui": ["2604562"], "spl_set_id": ["780907b8-34ba-4ec8-bcdf-b2a31bd111df"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "245.5 mL in 1 BOTTLE (0067-8205-01)", "package_ndc": "0067-8205-01", "marketing_start_date": "20220627"}], "brand_name": "Theraflu Flu Relief Max Strength Nighttime", "product_id": "0067-8205_446e5d67-95c9-e039-e063-6294a90a6cfa", "dosage_form": "SYRUP", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]"], "product_ndc": "0067-8205", "generic_name": "Acetaminophen, Chlorpheniramine maleate, Dextromethorphan HBr", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Theraflu Flu Relief Max Strength", "brand_name_suffix": "Nighttime", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "1000 mg/30mL"}, {"name": "CHLORPHENIRAMINE MALEATE", "strength": "4 mg/30mL"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "30 mg/30mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220627", "listing_expiration_date": "20261231"}