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POTASSIUM CHLORIDE EXTENDED RELEASE

NDC 70518-4520, POTASSIUM CHLORIDE, tablet, extended release, from REMEDYREPACK INC..

Product NDC
70518-4520
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA211797
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4520 \
  -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
70518-4520-07051845200030 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-4520-0)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d1e55181-6f85-42c9-922c-808494b6399a

Use it

Look up 70518-4520 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4520 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-4520. 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.