Package 68001-518-00

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 68001-518-00
Digits Only 6800151800
Product NDC 68001-518
Product ID 68001-518_eb3aa568-41e1-6c36-e053-2a95a90aa33a
Description

100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-518-00)

Marketing

Marketing Status
Marketed Since 2021-09-10
Brand potassium chloride
Generic potassium chloride
Sample Package No

Linked Drug Pages (1)

Potassium Chloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "eb3aa568-41e1-6c36-e053-2a95a90aa33a", "openfda": {"upc": ["0368001518000"], "unii": ["660YQ98I10"], "rxcui": ["628953"], "spl_set_id": ["73c911bb-4d39-4793-acba-90ed4b0eff46"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-518-00)", "package_ndc": "68001-518-00", "marketing_start_date": "20210910"}, {"sample": false, "description": "1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-518-08)", "package_ndc": "68001-518-08", "marketing_start_date": "20210910"}], "brand_name": "Potassium Chloride", "product_id": "68001-518_eb3aa568-41e1-6c36-e053-2a95a90aa33a", "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": "68001-518", "generic_name": "Potassium Chloride", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA210921", "marketing_category": "ANDA", "marketing_start_date": "20210910", "listing_expiration_date": "20261231"}