Package 70677-1005-1

Brand: sinus severe

Generic: acetaminophen, guaifenesin, and phenylephrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70677-1005-1
Digits Only 7067710051
Product NDC 70677-1005
Description

2 BLISTER PACK in 1 CARTON (70677-1005-1) / 12 TABLET, COATED in 1 BLISTER PACK

Marketing

Marketing Status
Discontinued 2027-03-31
Brand sinus severe
Generic acetaminophen, guaifenesin, and phenylephrine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "458c34d8-8e88-3178-e063-6394a90a3299", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1243679"], "spl_set_id": ["30d41dc3-e2ef-4cad-b63c-d634bc749aa1"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["STRATEGIC SOURCING SERVICES LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (70677-1005-1)  / 12 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "70677-1005-1", "marketing_end_date": "20270331", "marketing_start_date": "20230425"}], "brand_name": "Sinus Severe", "product_id": "70677-1005_458c34d8-8e88-3178-e063-6394a90a3299", "dosage_form": "TABLET, 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": "70677-1005", "generic_name": "ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE", "labeler_name": "STRATEGIC SOURCING SERVICES LLC", "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_end_date": "20270331", "marketing_start_date": "20230425"}