Package 17856-0048-3

{"route": ["ORAL"], "spl_id": "45af915d-a3d7-b59a-e063-6294a90ac162", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["312515"], "spl_set_id": ["dc55474c-cc51-4f17-8cb3-0f34b3e68a55"], "manufacturer_name": ["ATLANTIC BIOLOGICALS CORP."]}, "finished": true, "packaging": [{"sample": false, "description": "72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0048-1)  / 15 mL in 1 CUP, UNIT-DOSE (17856-0048-2)", "package_ndc": "17856-0048-1", "marketing_start_date": "20240711"}, {"sample": false, "description": "50 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0048-3)  / 30 mL in 1 CUP, UNIT-DOSE (17856-0048-4)", "package_ndc": "17856-0048-3", "marketing_start_date": "20240711"}], "brand_name": "POTASSIUM CHLORIDE", "product_id": "17856-0048_45af915d-a3d7-b59a-e063-6294a90ac162", "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": "17856-0048", "generic_name": "POTASSIUM CHLORIDE ORAL", "labeler_name": "ATLANTIC BIOLOGICALS CORP.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CHLORIDE", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "1.5 g/15mL"}], "application_number": "ANDA211648", "marketing_category": "ANDA", "marketing_start_date": "20231005", "listing_expiration_date": "20261231"}