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Potassium Acetate

NDC 51754-2004, Potassium Acetate, injection, from Exela Pharma Sciences, LLC.

Product NDC
51754-2004
Status
Listed
Labeler
Exela Pharma Sciences, LLC
Dosage form
INJECTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA206203
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51754-2004 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • POTASSIUM ACETATE200 meq/100mL

Pharmacologic 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]

Package NDCNDC-11Package
51754-2004-45175420040425 VIAL, GLASS in 1 CARTON (51754-2004-4) / 100 mL in 1 VIAL, GLASS

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d5f6dc05-9fb0-4a89-8c54-46112df10abd

Use it

Look up 51754-2004 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51754-2004 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51754-2004. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.