Package 50844-572-02
Brand: sinus severe
Generic: acetaminophen, guaifenesin, phenylephrine hclPackage Facts
Identity
Package NDC
50844-572-02
Digits Only
5084457202
Product NDC
50844-572
Description
1 BLISTER PACK in 1 CARTON (50844-572-02) / 12 TABLET, FILM COATED in 1 BLISTER PACK
Marketing
Marketing Status
Brand
sinus severe
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": "dc7e7b50-49a8-4d8b-98df-2f5edfb9d40d", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0350844572080"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1243679"], "spl_set_id": ["d5c8b248-6d82-4eac-881c-0b9d0a0de8f1"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["L.N.K. International, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (50844-572-02) / 12 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "50844-572-02", "marketing_start_date": "20210315"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (50844-572-08) / 12 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "50844-572-08", "marketing_start_date": "20210315"}], "brand_name": "Sinus Severe", "product_id": "50844-572_dc7e7b50-49a8-4d8b-98df-2f5edfb9d40d", "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": "50844-572", "generic_name": "Acetaminophen, Guaifenesin, Phenylephrine HCl", "labeler_name": "L.N.K. International, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sinus Severe", "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": "20210315", "listing_expiration_date": "20271231"}