Package 17856-1458-1
Brand: potassium chloride
Generic: potassium chloridePackage Facts
Identity
Package NDC
17856-1458-1
Digits Only
1785614581
Product NDC
17856-1458
Description
72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-1458-1) / 15 mL in 1 CUP, UNIT-DOSE
Marketing
Marketing Status
Brand
potassium chloride
Generic
potassium chloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "35cf03f4-1fe9-5643-e063-6394a90a9e02", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["314182"], "spl_set_id": ["104ccc91-2aaf-4bb7-bb64-77c29413f60e"], "manufacturer_name": ["ATLANTIC BIOLOGICALS CORP."]}, "finished": true, "packaging": [{"sample": false, "description": "72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-1458-1) / 15 mL in 1 CUP, UNIT-DOSE", "package_ndc": "17856-1458-1", "marketing_start_date": "20230920"}], "brand_name": "Potassium Chloride", "product_id": "17856-1458_35cf03f4-1fe9-5643-e063-6394a90a9e02", "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": "17856-1458", "generic_name": "Potassium Chloride", "labeler_name": "ATLANTIC BIOLOGICALS CORP.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "3 g/15mL"}], "application_number": "ANDA210041", "marketing_category": "ANDA", "marketing_start_date": "20180724", "listing_expiration_date": "20261231"}