Package 63868-747-24

{"route": ["ORAL"], "spl_id": "7e555b65-5cdd-2eb5-e053-2991aa0a8dce", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0635515987395"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1243679"], "spl_set_id": ["1e54ecb3-c3c3-477a-8725-23f24e77a44b"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Chain Drug Marketing Association"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (63868-747-24)  / 12 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "63868-747-24", "marketing_start_date": "20140521"}], "brand_name": "Pressure Pain Mucus PE", "product_id": "63868-747_7e555b65-5cdd-2eb5-e053-2991aa0a8dce", "dosage_form": "TABLET, COATED", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "63868-747", "generic_name": "ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE", "labeler_name": "Chain Drug Marketing Association", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pressure Pain Mucus PE", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "GUAIFENESIN", "strength": "200 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "part341", "marketing_category": "OTC MONOGRAPH FINAL", "marketing_start_date": "20140521", "listing_expiration_date": "20261231"}