Package 51316-549-06

Brand: theraflu relief max strength nighttime

Generic: acetaminophen, chlorpheniramine maleate and dextromethophan hbr
NDC Package

Package Facts

Identity

Package NDC 51316-549-06
Digits Only 5131654906
Product NDC 51316-549
Product ID 51316-549_456f5b3a-842f-e145-e063-6394a90aa4d9
Description

1 POWDER, FOR SOLUTION in 1 PACKET (51316-549-06)

Marketing

Marketing Status
Marketed Since 2023-04-17
Brand theraflu relief max strength nighttime
Generic acetaminophen, chlorpheniramine maleate and dextromethophan hbr
Sample Package No

Linked Drug Pages (1)

Theraflu Relief Max Strength Nighttime ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "456f5b3a-842f-e145-e063-6394a90aa4d9", "openfda": {"unii": ["362O9ITL9D", "V1Q0O9OJ9Z", "9D2RTI9KYH"], "rxcui": ["2636658"], "spl_set_id": ["4b567234-1da9-4e10-a427-877eea2be1c1"], "manufacturer_name": ["CVS PHARMACY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 POWDER, FOR SOLUTION in 1 PACKET (51316-549-06)", "package_ndc": "51316-549-06", "marketing_start_date": "20230417"}], "brand_name": "Theraflu Relief Max Strength Nighttime", "product_id": "51316-549_456f5b3a-842f-e145-e063-6394a90aa4d9", "dosage_form": "POWDER, FOR SOLUTION", "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": "51316-549", "generic_name": "Acetaminophen, Chlorpheniramine Maleate and Dextromethophan HBr", "labeler_name": "CVS PHARMACY", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Theraflu Relief Max Strength", "brand_name_suffix": "Nighttime", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "1000 mg/1"}, {"name": "CHLORPHENIRAMINE MALEATE", "strength": "4 mg/1"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "30 mg/1"}], "application_number": "M010", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230417", "listing_expiration_date": "20261231"}