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Potassium Chloride

NDC 50268-675, Potassium Chloride, solution, from AvPAK.

Product NDC
50268-675
Status
Listed
Labeler
AvPAK
Dosage form
SOLUTION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA210041
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50268-675 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • POTASSIUM CHLORIDE3 g/15mL

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
50268-675-125026806751220 CUP in 1 BOX (50268-675-12) / 15 mL in 1 CUP (50268-675-11)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f32df7c0-33eb-e6d6-e053-2a95a90a2e8d

Use it

Look up 50268-675 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50268-675 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50268-675. 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.