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Potassium Chloride

NDC 50090-6635, potassium chloride, tablet, film coated, extended release, from A-S Medication Solutions.

Product NDC
50090-6635
Status
Listed
Labeler
A-S Medication Solutions
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204662
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50090-6635 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • POTASSIUM CHLORIDE10 meq/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
50090-6635-05009066350090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6635-0)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f1af7e05-68ba-438e-a63b-cd8c23960c85

Use it

Look up 50090-6635 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50090-6635 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50090-6635. 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.