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Potassium Chloride Extended-release

NDC 17856-1135, Potassium Chloride Extended-release, tablet, extended release, from Atlantic Biologicals Corp..

Product NDC
17856-1135
Status
Listed
Labeler
Atlantic Biologicals Corp.
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA214452
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/17856-1135 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • POTASSIUM CHLORIDE1500 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
17856-1135-117856113501100 POUCH in 1 BOX, UNIT-DOSE (17856-1135-1) / 1 TABLET, EXTENDED RELEASE in 1 POUCH

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4d7ad5c6-2c18-dc29-e063-6394a90a621e

Use it

Look up 17856-1135 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/17856-1135 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 17856-1135. 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.