Package 68462-472-01

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 68462-472-01
Digits Only 6846247201
Product NDC 68462-472
Product ID 68462-472_1ee2b3cb-f4b4-4efc-a7a2-3be15cf4b6cc
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68462-472-01)

Marketing

Marketing Status
Marketed Since 2016-07-26
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": "1ee2b3cb-f4b4-4efc-a7a2-3be15cf4b6cc", "openfda": {"upc": ["0368462471012", "0368462472019"], "unii": ["660YQ98I10"], "rxcui": ["1801294", "1801298"], "spl_set_id": ["63bedd99-0596-49d2-ad04-d1d8ac15cc42"], "manufacturer_name": ["Glenmark Pharmaceuticals Inc., USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68462-472-01)", "package_ndc": "68462-472-01", "marketing_start_date": "20160726"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68462-472-05)", "package_ndc": "68462-472-05", "marketing_start_date": "20160726"}], "brand_name": "potassium chloride", "product_id": "68462-472_1ee2b3cb-f4b4-4efc-a7a2-3be15cf4b6cc", "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": "68462-472", "generic_name": "potassium chloride", "labeler_name": "Glenmark Pharmaceuticals Inc., USA", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "potassium chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "1500 mg/1"}], "application_number": "ANDA203562", "marketing_category": "ANDA", "marketing_start_date": "20160726", "listing_expiration_date": "20261231"}