Package 0135-0607-03

{"route": ["ORAL"], "spl_id": "10c08cd4-8a3b-c9ad-e063-6394a90a9641", "openfda": {"unii": ["362O9ITL9D", "04JA59TNSJ"], "rxcui": ["1046378"], "spl_set_id": ["f626ab17-01c9-4493-ba9e-0c8c11146384"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (0135-0607-02)  / 8 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0135-0607-02", "marketing_start_date": "20170601"}, {"sample": false, "description": "50 PACKET in 1 CARTON (0135-0607-03)  / 2 TABLET, FILM COATED in 1 PACKET (0135-0607-01)", "package_ndc": "0135-0607-03", "marketing_start_date": "20170601"}], "brand_name": "Panadol Cold and Flu NonDrowsy", "product_id": "0135-0607_10c08cd4-8a3b-c9ad-e063-6394a90a9641", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "0135-0607", "generic_name": "acetaminophen and phenyleprine HCl", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Panadol", "brand_name_suffix": "Cold and Flu NonDrowsy", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20170601", "listing_expiration_date": "20261231"}