Package 55319-815-19

Brand: severe congestion and pain

Generic: acetaminophen, guaifenesin, phenylephrine hcl
NDC Package

Package Facts

Identity

Package NDC 55319-815-19
Digits Only 5531981519
Product NDC 55319-815
Description

1 BLISTER PACK in 1 CARTON (55319-815-19) / 8 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2023-12-13
Brand severe congestion and pain
Generic acetaminophen, guaifenesin, phenylephrine hcl
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "65750131-b822-4b6a-943b-1f460acdbe01", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0032251923968"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1243679"], "spl_set_id": ["ce590997-3cae-4f22-ac39-2b14d39494bc"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Family Dollar Services Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (55319-815-19)  / 8 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "55319-815-19", "marketing_start_date": "20231213"}], "brand_name": "Severe Congestion and Pain", "product_id": "55319-815_65750131-b822-4b6a-943b-1f460acdbe01", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "55319-815", "generic_name": "Acetaminophen, Guaifenesin, Phenylephrine HCl", "labeler_name": "Family Dollar Services Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Severe Congestion and Pain", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "GUAIFENESIN", "strength": "200 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20231213", "listing_expiration_date": "20261231"}