Package 63739-724-50

{"route": ["ORAL"], "spl_id": "99de73d1-2a10-4dab-b2da-b245b79452d6", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["312515"], "spl_set_id": ["fc70ccc0-416e-4109-af22-6c6f00da5906"], "manufacturer_name": ["McKesson Corporation dba SKY Packaging"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 TRAY in 1 CASE (63739-724-50)  / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (63739-724-01)", "package_ndc": "63739-724-50", "marketing_end_date": "20260731", "marketing_start_date": "20230825"}], "brand_name": "Potassium Chloride", "product_id": "63739-724_99de73d1-2a10-4dab-b2da-b245b79452d6", "dosage_form": "SOLUTION", "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": "63739-724", "generic_name": "POTASSIUM CHLORIDE", "labeler_name": "McKesson Corporation dba SKY Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "20 meq/15mL"}], "application_number": "ANDA210766", "marketing_category": "ANDA", "marketing_end_date": "20260731", "marketing_start_date": "20230825"}