Package 0378-4561-05
Brand: potassium chloride
Generic: potassium chloridePackage Facts
Identity
Package NDC
0378-4561-05
Digits Only
0378456105
Product NDC
0378-4561
Description
500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-4561-05)
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": "a05e4397-8442-41d9-afa7-832163c3b554", "openfda": {"upc": ["0303784561775", "0303784560778"], "unii": ["660YQ98I10"], "rxcui": ["312529", "628953"], "spl_set_id": ["c64ed4c0-1e27-42b3-9625-fb4e0d31e271"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-4561-05)", "package_ndc": "0378-4561-05", "marketing_end_date": "20270131", "marketing_start_date": "20161109"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-4561-77)", "package_ndc": "0378-4561-77", "marketing_end_date": "20261130", "marketing_start_date": "20161109"}], "brand_name": "Potassium Chloride", "product_id": "0378-4561_a05e4397-8442-41d9-afa7-832163c3b554", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "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": "0378-4561", "generic_name": "potassium chloride", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "10 meq/1"}], "application_number": "ANDA204662", "marketing_category": "ANDA", "marketing_end_date": "20270131", "marketing_start_date": "20161109"}