potassium acetate

Generic: potassium acetate

Labeler: hospira, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium acetate
Generic Name potassium acetate
Labeler hospira, inc.
Dosage Form INJECTION, SOLUTION, CONCENTRATE
Routes
INTRAVENOUS
Active Ingredients

potassium acetate 3.93 g/20mL

Manufacturer
Hospira, Inc.

Identifiers & Regulatory

Product NDC 0409-8183
Product ID 0409-8183_32342707-1d72-4fa4-813c-0cc998c95c16
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA018896
Listing Expiration 2026-12-31
Marketing Start 2005-07-07

Pharmacologic Class

Classes
increased large intestinal motility [pe] inhibition large intestine fluid/electrolyte absorption [pe] osmotic activity [moa] osmotic laxative [epc] potassium compounds [cs] potassium salt [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 04098183
Hyphenated Format 0409-8183

Supplemental Identifiers

RxCUI
1871155
UNII
M911911U02

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name potassium acetate (source: ndc)
Generic Name potassium acetate (source: ndc)
Application Number NDA018896 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 3.93 g/20mL
source: ndc
Packaging
  • 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-8183-01) / 20 mL in 1 VIAL, SINGLE-DOSE (0409-8183-11)
source: ndc

Packages (1)

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

Ingredients (1)

potassium acetate (3.93 g/20mL)

Linked Drug Pages (2)

Potassium Acetate ndc-match (0.9) Potassium Acetate ndc-match (0.9)

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"}