Package 72603-337-01

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 72603-337-01
Digits Only 7260333701
Product NDC 72603-337
Product ID 72603-337_2087e0c5-7d3f-48dd-823d-5b4f72beb998
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72603-337-01)

Marketing

Marketing Status
Marketed Since 2024-06-21
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": "2087e0c5-7d3f-48dd-823d-5b4f72beb998", "openfda": {"upc": ["0372603337013"], "unii": ["660YQ98I10"], "rxcui": ["1801294", "1801298"], "spl_set_id": ["b19a3fbf-cdbb-4f86-ac61-5dfb07e0a51a"], "manufacturer_name": ["Northstar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72603-337-01)", "package_ndc": "72603-337-01", "marketing_start_date": "20240621"}], "brand_name": "potassium chloride", "product_id": "72603-337_2087e0c5-7d3f-48dd-823d-5b4f72beb998", "dosage_form": "TABLET, 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": "72603-337", "generic_name": "potassium chloride", "labeler_name": "Northstar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "potassium chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA214422", "marketing_category": "ANDA", "marketing_start_date": "20240621", "listing_expiration_date": "20261231"}