Package 68382-740-01

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 68382-740-01
Digits Only 6838274001
Product NDC 68382-740
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-740-01)

Marketing

Marketing Status
Marketed Since 2022-02-03
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": "5e98c67f-9957-446f-bcf6-4ed08def954f", "openfda": {"upc": ["0368382861016", "0368382740014"], "unii": ["660YQ98I10"], "rxcui": ["1801294", "1801298"], "spl_set_id": ["31e02249-7984-4b8f-9e37-2b79b708ac08"], "manufacturer_name": ["Zydus Pharmaceuticals (USA) Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-740-01)", "package_ndc": "68382-740-01", "marketing_start_date": "20220203"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-740-05)", "package_ndc": "68382-740-05", "marketing_start_date": "20220203"}, {"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-740-10)", "package_ndc": "68382-740-10", "marketing_start_date": "20220203"}], "brand_name": "Potassium Chloride", "product_id": "68382-740_5e98c67f-9957-446f-bcf6-4ed08def954f", "dosage_form": "TABLET, EXTENDED RELEASE", "product_ndc": "68382-740", "generic_name": "Potassium Chloride", "labeler_name": "Zydus Pharmaceuticals (USA) Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "1500 mg/1"}], "application_number": "ANDA210395", "marketing_category": "ANDA", "marketing_start_date": "20220203", "listing_expiration_date": "20261231"}