Package 0067-7921-02

Brand: theraflu flu relief max strength daytime

Generic: acetaminophen, dextromethorphan hbr
NDC Package

Package Facts

Identity

Package NDC 0067-7921-02
Digits Only 0067792102
Product NDC 0067-7921
Description

6 POWDER in 1 CARTON (0067-7921-02)

Marketing

Marketing Status
Marketed Since 2022-06-15
Brand theraflu flu relief max strength daytime
Generic acetaminophen, dextromethorphan hbr
Sample Package No

Linked Drug Pages (2)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "35339df5-9ec8-6a29-e063-6294a90acbb9", "openfda": {"unii": ["362O9ITL9D", "9D2RTI9KYH"], "rxcui": ["2636656"], "spl_set_id": ["a1405038-80f2-45e5-bd8c-8c6b0ee348be"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 POWDER in 1 CARTON (0067-7921-02)", "package_ndc": "0067-7921-02", "marketing_start_date": "20220615"}], "brand_name": "Theraflu Flu Relief Max Strength Daytime", "product_id": "0067-7921_35339df5-9ec8-6a29-e063-6294a90acbb9", "dosage_form": "POWDER", "pharm_class": ["Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]"], "product_ndc": "0067-7921", "generic_name": "Acetaminophen, Dextromethorphan HBr", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Theraflu Flu Relief Max Strength", "brand_name_suffix": "Daytime", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "1000 mg/1"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "30 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220615", "listing_expiration_date": "20261231"}