Package 72189-027-04

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 72189-027-04
Digits Only 7218902704
Product NDC 72189-027
Product ID 72189-027_2c4e994c-a009-5fc9-e063-6294a90a462a
Description

4 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-027-04)

Marketing

Marketing Status
Marketed Since 2019-10-02
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": "2c4e994c-a009-5fc9-e063-6294a90a462a", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["628953"], "spl_set_id": ["946b9568-671d-172a-e053-2a95a90ac827"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "4 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-027-04)", "package_ndc": "72189-027-04", "marketing_start_date": "20191002"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-027-30)", "package_ndc": "72189-027-30", "marketing_start_date": "20191002"}], "brand_name": "POTASSIUM CHLORIDE", "product_id": "72189-027_2c4e994c-a009-5fc9-e063-6294a90a462a", "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": "72189-027", "generic_name": "POTASSIUM CHLORIDE", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CHLORIDE", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA210733", "marketing_category": "ANDA", "marketing_start_date": "20191002", "listing_expiration_date": "20261231"}