Package 70436-153-01

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 70436-153-01
Digits Only 7043615301
Product NDC 70436-153
Description

100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70436-153-01)

Marketing

Marketing Status
Marketed Since 2020-02-01
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": "3bc1f760-5a34-e736-e063-6394a90ab638", "openfda": {"upc": ["0370436153015", "0370436152018"], "unii": ["660YQ98I10"], "rxcui": ["198116", "628953"], "spl_set_id": ["94ae03cc-b620-0dbb-e053-2a95a90a922c"], "manufacturer_name": ["Slate Run Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70436-153-01)", "package_ndc": "70436-153-01", "marketing_start_date": "20200201"}, {"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70436-153-02)", "package_ndc": "70436-153-02", "marketing_start_date": "20200201"}], "brand_name": "Potassium Chloride", "product_id": "70436-153_3bc1f760-5a34-e736-e063-6394a90ab638", "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": "70436-153", "generic_name": "Potassium Chloride", "labeler_name": "Slate Run Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "1500 mg/1"}], "application_number": "ANDA212561", "marketing_category": "ANDA", "marketing_start_date": "20200201", "listing_expiration_date": "20261231"}