Package 71656-022-50

{"route": ["ORAL"], "spl_id": "4872fd4b-ae1d-9c4c-e063-6294a90a7fc6", "openfda": {"upc": ["0371656021160"], "unii": ["660YQ98I10"], "rxcui": ["312515", "314182"], "spl_set_id": ["483f338e-a164-4c1f-a34e-fef3312cb7ec"], "manufacturer_name": ["Saptalis Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 TRAY in 1 CASE (71656-022-01)  / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (71656-022-15)", "package_ndc": "71656-022-01", "marketing_start_date": "20231005"}, {"sample": false, "description": "473 mL in 1 BOTTLE (71656-022-16)", "package_ndc": "71656-022-16", "marketing_start_date": "20231005"}, {"sample": false, "description": "5 TRAY in 1 CASE (71656-022-50)  / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (71656-022-15)", "package_ndc": "71656-022-50", "marketing_start_date": "20231005"}], "brand_name": "POTASSIUM CHLORIDE", "product_id": "71656-022_4872fd4b-ae1d-9c4c-e063-6294a90a7fc6", "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": "71656-022", "generic_name": "POTASSIUM CHLORIDE", "labeler_name": "Saptalis Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CHLORIDE", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "3 g/15mL"}], "application_number": "ANDA211648", "marketing_category": "ANDA", "marketing_start_date": "20231005", "listing_expiration_date": "20271231"}