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Potassium Chloride

NDC 68382-740, Potassium Chloride, tablet, extended release, from Zydus Pharmaceuticals (USA) Inc..

Product NDC
68382-740
Status
Listed
Labeler
Zydus Pharmaceuticals (USA) Inc.
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA210395
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68382-740 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • POTASSIUM CHLORIDE1500 mg/1
Package NDCNDC-11Package
68382-740-0168382074001100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-740-01)
68382-740-0568382074005500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-740-05)
68382-740-10683820740101000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-740-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/31e02249-7984-4b8f-9e37-2b79b708ac08

Use it

Look up 68382-740 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68382-740 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68382-740. 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.