Package 21130-399-01

{"route": ["ORAL"], "spl_id": "9a157898-5c65-40f7-9795-c583386668c8", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["495W7451VQ"], "rxcui": ["310621"], "spl_set_id": ["8b981962-5724-47d0-81f5-945dea169943"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Better Living Brands, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (21130-399-01)  / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "21130-399-01", "marketing_start_date": "20200717"}], "brand_name": "MUCUS RELIEF MAX", "product_id": "21130-399_9a157898-5c65-40f7-9795-c583386668c8", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "21130-399", "generic_name": "Guaifenesin", "labeler_name": "Better Living Brands, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "MUCUS RELIEF MAX", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "1200 mg/1"}], "application_number": "ANDA210453", "marketing_category": "ANDA", "marketing_start_date": "20200717", "listing_expiration_date": "20261231"}