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Potassium Chloride

NDC 70436-152, Potassium Chloride, tablet, film coated, extended release, from Slate Run Pharmaceuticals, LLC.

Product NDC
70436-152
Status
Listed
Labeler
Slate Run Pharmaceuticals, LLC
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA212561
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70436-152 \
  -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
70436-152-0170436015201100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70436-152-01)
70436-152-03704360152031000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70436-152-03)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/94ae03cc-b620-0dbb-e053-2a95a90a922c

Use it

Look up 70436-152 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70436-152 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70436-152. 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.