Package 80513-303-50

Brand: daytime cold and flu relief

Generic: acetaminophen, dextromethorphan hydrobromide, and phenylephrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 80513-303-50
Digits Only 8051330350
Product NDC 80513-303
Product ID 80513-303_14dd3fc0-c0c1-38d3-e063-6394a90a3dcc
Description

50 CAPSULE, LIQUID FILLED in 1 BOTTLE (80513-303-50)

Marketing

Marketing Status
Marketed Since 2024-03-01
Brand daytime cold and flu relief
Generic acetaminophen, dextromethorphan hydrobromide, and phenylephrine hydrochloride
Sample Package No

Linked Drug Pages (1)

DAYTIME COLD AND FLU RELIEF ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "14dd3fc0-c0c1-38d3-e063-6394a90a3dcc", "openfda": {"unii": ["362O9ITL9D", "9D2RTI9KYH", "04JA59TNSJ"], "rxcui": ["1086997"], "spl_set_id": ["38299cf3-e884-4676-8cc4-6dd64e7d023c"], "manufacturer_name": ["Advanced Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 CAPSULE, LIQUID FILLED in 1 BOTTLE (80513-303-50)", "package_ndc": "80513-303-50", "marketing_start_date": "20240301"}], "brand_name": "DAYTIME COLD AND FLU RELIEF", "product_id": "80513-303_14dd3fc0-c0c1-38d3-e063-6394a90a3dcc", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "80513-303", "generic_name": "Acetaminophen, Dextromethorphan Hydrobromide, and Phenylephrine Hydrochloride", "labeler_name": "Advanced Rx LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "DAYTIME COLD AND FLU RELIEF", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "10 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240301", "listing_expiration_date": "20261231"}