Package 81033-240-51
Brand: potassium chloride
Generic: potassium chloridePackage Facts
Identity
Package NDC
81033-240-51
Digits Only
8103324051
Product NDC
81033-240
Description
10 TRAY in 1 CASE (81033-240-51) / 10 CUP, UNIT-DOSE in 1 TRAY / 30 mL in 1 CUP, UNIT-DOSE (81033-240-30)
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": "137da9b4-83f0-355f-e063-6294a90af512", "openfda": {"upc": ["0381033220512", "0381033220529", "0381033240510", "0381033240503"], "unii": ["660YQ98I10"], "rxcui": ["312515"], "spl_set_id": ["25c2b417-eeea-4ba6-8eb9-a7d8a08c6093"], "manufacturer_name": ["Kesin Pharma Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 TRAY in 1 CASE (81033-240-50) / 10 CUP, UNIT-DOSE in 1 TRAY / 30 mL in 1 CUP, UNIT-DOSE (81033-240-30)", "package_ndc": "81033-240-50", "marketing_start_date": "20220815"}, {"sample": false, "description": "10 TRAY in 1 CASE (81033-240-51) / 10 CUP, UNIT-DOSE in 1 TRAY / 30 mL in 1 CUP, UNIT-DOSE (81033-240-30)", "package_ndc": "81033-240-51", "marketing_start_date": "20220815"}], "brand_name": "POTASSIUM CHLORIDE", "product_id": "81033-240_137da9b4-83f0-355f-e063-6294a90af512", "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": "81033-240", "generic_name": "POTASSIUM CHLORIDE", "labeler_name": "Kesin Pharma Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CHLORIDE", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "3 g/30mL"}], "application_number": "ANDA211648", "marketing_category": "ANDA", "marketing_start_date": "20220815", "listing_expiration_date": "20261231"}