potassium acetate

Generic: potassium acetate

Labeler: exela pharma sciences, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium acetate
Generic Name potassium acetate
Labeler exela pharma sciences, llc
Dosage Form INJECTION
Routes
INTRAVENOUS
Active Ingredients

potassium acetate 200 meq/100mL

Manufacturer
Exela Pharma Sciences, LLC

Identifiers & Regulatory

Product NDC 51754-2004
Product ID 51754-2004_2b86b9e8-48ba-4a72-b705-48c2751016e6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206203
Listing Expiration 2026-12-31
Marketing Start 2023-08-01

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 517542004
Hyphenated Format 51754-2004

Supplemental Identifiers

RxCUI
237381
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 ANDA206203 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 200 meq/100mL
source: ndc
Packaging
  • 25 VIAL, GLASS in 1 CARTON (51754-2004-4) / 100 mL in 1 VIAL, GLASS
source: ndc

Packages (1)

51754-2004-4 25 VIAL, GLASS in 1 CARTON (51754-2004-4) / 100 mL in 1 VIAL, GLASS

Ingredients (1)

potassium acetate (200 meq/100mL)

Linked Drug Pages (1)

Potassium Acetate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "2b86b9e8-48ba-4a72-b705-48c2751016e6", "openfda": {"unii": ["M911911U02"], "rxcui": ["237381"], "spl_set_id": ["d5f6dc05-9fb0-4a89-8c54-46112df10abd"], "manufacturer_name": ["Exela Pharma Sciences, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, GLASS in 1 CARTON (51754-2004-4)  / 100 mL in 1 VIAL, GLASS", "package_ndc": "51754-2004-4", "marketing_start_date": "20230801"}], "brand_name": "Potassium Acetate", "product_id": "51754-2004_2b86b9e8-48ba-4a72-b705-48c2751016e6", "dosage_form": "INJECTION", "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": "51754-2004", "generic_name": "Potassium Acetate", "labeler_name": "Exela Pharma Sciences, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Acetate", "active_ingredients": [{"name": "POTASSIUM ACETATE", "strength": "200 meq/100mL"}], "application_number": "ANDA206203", "marketing_category": "ANDA", "marketing_start_date": "20230801", "listing_expiration_date": "20261231"}