Package 51655-568-52

{"route": ["ORAL"], "spl_id": "494e12ac-cf8c-6058-e063-6294a90ada50", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1801294"], "spl_set_id": ["dae7c63d-eef0-58d0-e053-2a95a90a667e"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-568-25)", "package_ndc": "51655-568-25", "marketing_start_date": "20230213"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-568-26)", "package_ndc": "51655-568-26", "marketing_start_date": "20221031"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-568-52)", "package_ndc": "51655-568-52", "marketing_start_date": "20210128"}, {"sample": false, "description": "45 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-568-90)", "package_ndc": "51655-568-90", "marketing_start_date": "20230306"}], "brand_name": "Potassium Chloride", "product_id": "51655-568_494e12ac-cf8c-6058-e063-6294a90ada50", "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": "51655-568", "generic_name": "potassium chloride", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "1500 mg/1"}], "application_number": "ANDA074726", "marketing_category": "ANDA", "marketing_start_date": "20210128", "listing_expiration_date": "20271231"}