Package 0409-6651-06

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 0409-6651-06
Digits Only 0409665106
Product NDC 0409-6651
Product ID 0409-6651_51305788-d1bb-4fef-86a7-6e62f7b01f00
Description

25 VIAL, SINGLE-DOSE in 1 TRAY (0409-6651-06) / 10 mL in 1 VIAL, SINGLE-DOSE (0409-6651-19)

Marketing

Marketing Status
Marketed Since 2005-11-10
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": ["INTRAVENOUS"], "spl_id": "51305788-d1bb-4fef-86a7-6e62f7b01f00", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1860132", "1860136", "1860139"], "spl_set_id": ["559a0a8c-a8fe-40a5-b196-21f9308780ab"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 TRAY (0409-6651-06)  / 10 mL in 1 VIAL, SINGLE-DOSE (0409-6651-19)", "package_ndc": "0409-6651-06", "marketing_start_date": "20051110"}], "brand_name": "POTASSIUM CHLORIDE", "product_id": "0409-6651_51305788-d1bb-4fef-86a7-6e62f7b01f00", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "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": "0409-6651", "generic_name": "POTASSIUM CHLORIDE", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CHLORIDE", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "149 mg/mL"}], "application_number": "ANDA080205", "marketing_category": "ANDA", "marketing_start_date": "20051110", "listing_expiration_date": "20271231"}