Package 55154-6709-0

{"route": ["ORAL"], "spl_id": "48bda54d-9d59-46cd-bd32-fa89ef93c1b7", "openfda": {"upc": ["0055154670906"], "unii": ["660YQ98I10"], "rxcui": ["628953"], "spl_set_id": ["446ad1bd-cf5c-41a7-945f-a6575cab16bf"], "manufacturer_name": ["Cardinal Health 107, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BAG (55154-6709-0)  / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "55154-6709-0", "marketing_end_date": "20260531", "marketing_start_date": "20160505"}], "brand_name": "Potassium chloride extended release", "product_id": "55154-6709_48bda54d-9d59-46cd-bd32-fa89ef93c1b7", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Potassium Compounds [CS]", "Potassium Salt [EPC]"], "product_ndc": "55154-6709", "generic_name": "Potassium chloride", "labeler_name": "Cardinal Health 107, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium chloride extended release", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "10 meq/1"}], "application_number": "ANDA205993", "marketing_category": "ANDA", "marketing_end_date": "20260531", "marketing_start_date": "20151211"}