Package 68001-619-03

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 68001-619-03
Digits Only 6800161903
Product NDC 68001-619
Product ID 68001-619_42ebb029-df0e-9096-e063-6294a90a9dcc
Description

500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68001-619-03)

Marketing

Marketing Status
Marketed Since 2024-07-10
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": "42ebb029-df0e-9096-e063-6294a90a9dcc", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["312504"], "spl_set_id": ["3709ee9a-f885-4a75-ab51-36e9e1ef0427"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68001-619-00)", "package_ndc": "68001-619-00", "marketing_start_date": "20240710"}, {"sample": false, "description": "500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68001-619-03)", "package_ndc": "68001-619-03", "marketing_start_date": "20240710"}], "brand_name": "Potassium Chloride", "product_id": "68001-619_42ebb029-df0e-9096-e063-6294a90a9dcc", "dosage_form": "CAPSULE, 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": "68001-619", "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": "ANDA214686", "marketing_category": "ANDA", "marketing_start_date": "20240710", "listing_expiration_date": "20261231"}