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Potassium Citrate

NDC 68382-536, Potassium Citrate, tablet, extended release, from Zydus Pharmaceuticals (USA) Inc..

Product NDC
68382-536
Status
Listed
Labeler
Zydus Pharmaceuticals (USA) Inc.
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203546
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68382-536 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • POTASSIUM CITRATE5 meq/1

Pharmacologic classes

Acidifying Activity [MoA]; Anti-coagulant [EPC]; Calcium Chelating Activity [MoA]; Calculi Dissolution Agent [EPC]; Decreased Coagulation Factor Activity [PE]

Package NDCNDC-11Package
68382-536-0168382053601100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-536-01)
68382-536-0568382053605500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-536-05)
68382-536-066838205360630 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-536-06)
68382-536-10683820536101000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-536-10)
68382-536-166838205361690 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-536-16)
68382-536-306838205363010 BLISTER PACK in 1 CARTON (68382-536-30) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1a839f91-9bbd-4f46-b350-c5e8074b5db7

  • NADAC price for package 68382053601

    GET /v1/drugs/nadac/68382053601

Use it

Look up 68382-536 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68382-536 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68382-536. 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.