Package 62011-0475-1

Brand: guaifenesin and pseudoephedrine hydrochloride

Generic: guaifenesin and pseudoephedrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 62011-0475-1
Digits Only 6201104751
Product NDC 62011-0475
Description

1 BLISTER PACK in 1 CARTON (62011-0475-1) / 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2017-12-10
Brand guaifenesin and pseudoephedrine hydrochloride
Generic guaifenesin and pseudoephedrine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "07be87a3-54dc-4ddb-bd01-45444b4cf0ac", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["495W7451VQ", "6V9V2RYJ8N"], "rxcui": ["1305603"], "spl_set_id": ["d139fd8d-66fd-4484-8e78-ed90c505d999"], "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": "1 BLISTER PACK in 1 CARTON (62011-0475-1)  / 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "62011-0475-1", "marketing_start_date": "20171210"}], "brand_name": "Guaifenesin and Pseudoephedrine Hydrochloride", "product_id": "62011-0475_07be87a3-54dc-4ddb-bd01-45444b4cf0ac", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "62011-0475", "generic_name": "Guaifenesin and Pseudoephedrine Hydrochloride", "labeler_name": "STRATEGIC SOURCING SERVICES LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Guaifenesin and Pseudoephedrine Hydrochloride", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "600 mg/1"}, {"name": "PSEUDOEPHEDRINE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA212542", "marketing_category": "ANDA", "marketing_start_date": "20171115", "listing_expiration_date": "20261231"}