Package 37808-935-40

{"route": ["ORAL"], "spl_id": "884b612b-7aff-4e32-aa00-a77e28346a7f", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0041220148134"], "unii": ["495W7451VQ"], "rxcui": ["636522"], "spl_set_id": ["562b6ab6-4795-4909-8008-e919173844c9"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (37808-935-40)  / 40 TABLET in 1 BOTTLE, PLASTIC", "package_ndc": "37808-935-40", "marketing_start_date": "20210528"}], "brand_name": "Mucus Relief", "product_id": "37808-935_884b612b-7aff-4e32-aa00-a77e28346a7f", "dosage_form": "TABLET", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "37808-935", "generic_name": "Guaifenesin", "labeler_name": "H E B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "600 mg/1"}], "application_number": "ANDA207342", "marketing_category": "ANDA", "marketing_start_date": "20210528", "listing_expiration_date": "20261231"}