Package 50090-6640-0

{"route": ["ORAL"], "spl_id": "02101932-08ca-4069-a6b2-b182eea53269", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["628953"], "spl_set_id": ["0dc6c066-1a59-4798-b9e6-d66872245389"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6640-0)", "package_ndc": "50090-6640-0", "marketing_start_date": "20230829"}], "brand_name": "Potassium Chloride Extended-Release", "product_id": "50090-6640_02101932-08ca-4069-a6b2-b182eea53269", "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": "50090-6640", "generic_name": "Potassium Chloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "brand_name_suffix": "Extended-Release", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA209688", "marketing_category": "ANDA", "marketing_start_date": "20230410", "listing_expiration_date": "20261231"}