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Potassium Chloride

NDC 67046-1032, Potassium Chloride, tablet, film coated, extended release, from Coupler LLC.

Product NDC
67046-1032
Status
Listed
Labeler
Coupler LLC
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA210921
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/67046-1032 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • POTASSIUM CHLORIDE750 mg/1

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
67046-1032-36704610320330 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (67046-1032-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/598f61d7-a665-5d02-e063-6394a90a8905

Use it

Look up 67046-1032 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/67046-1032 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 67046-1032. 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.