Package 0409-8183-01

Brand: potassium acetate

Generic: potassium acetate
NDC Package

Package Facts

Identity

Package NDC 0409-8183-01
Digits Only 0409818301
Product NDC 0409-8183
Product ID 0409-8183_32342707-1d72-4fa4-813c-0cc998c95c16
Description

25 VIAL, SINGLE-DOSE in 1 TRAY (0409-8183-01) / 20 mL in 1 VIAL, SINGLE-DOSE (0409-8183-11)

Marketing

Marketing Status
Marketed Since 2005-07-07
Brand potassium acetate
Generic potassium acetate
Sample Package No

Linked Drug Pages (1)

Potassium Acetate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "32342707-1d72-4fa4-813c-0cc998c95c16", "openfda": {"unii": ["M911911U02"], "rxcui": ["1871155"], "spl_set_id": ["8123cce8-42e3-49e4-a488-3bb836ecccd0"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 TRAY (0409-8183-01)  / 20 mL in 1 VIAL, SINGLE-DOSE (0409-8183-11)", "package_ndc": "0409-8183-01", "marketing_start_date": "20050707"}], "brand_name": "Potassium Acetate", "product_id": "0409-8183_32342707-1d72-4fa4-813c-0cc998c95c16", "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": "0409-8183", "generic_name": "POTASSIUM ACETATE", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Acetate", "active_ingredients": [{"name": "POTASSIUM ACETATE", "strength": "3.93 g/20mL"}], "application_number": "NDA018896", "marketing_category": "NDA", "marketing_start_date": "20050707", "listing_expiration_date": "20261231"}