Package 37808-830-20

{"route": ["ORAL"], "spl_id": "b74e7c92-7fe7-4455-9af9-6ebe568639b7", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0041220831890"], "unii": ["495W7451VQ"], "rxcui": ["636522"], "spl_set_id": ["efebda97-5234-451c-a854-91a32303a6b7"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["H E B"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (37808-830-20)  / 20 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC", "package_ndc": "37808-830-20", "marketing_start_date": "20230605"}], "brand_name": "Mucus Relief", "product_id": "37808-830_b74e7c92-7fe7-4455-9af9-6ebe568639b7", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "37808-830", "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": "20230605", "listing_expiration_date": "20261231"}