Package 72036-204-02

{"route": ["ORAL"], "spl_id": "1adad3a9-6060-7cb9-e063-6294a90a7acd", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["495W7451VQ"], "rxcui": ["310621"], "spl_set_id": ["114a8c26-25be-5a0b-e063-6294a90a3e18"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["HARRIS TEETER"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (72036-204-02)  / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "72036-204-02", "marketing_start_date": "20240301"}], "brand_name": "Mucus Relief Maximum Strength", "product_id": "72036-204_1adad3a9-6060-7cb9-e063-6294a90a7acd", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "72036-204", "generic_name": "Guaifenesin", "labeler_name": "HARRIS TEETER", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief", "brand_name_suffix": "Maximum Strength", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "1200 mg/1"}], "application_number": "ANDA213420", "marketing_category": "ANDA", "marketing_start_date": "20240301", "listing_expiration_date": "20261231"}