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Potassium Citrate

NDC 72162-1759, Potassium Citrate, tablet, extended release, from Bryant Ranch Prepack.

Product NDC
72162-1759
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA212779
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72162-1759 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • POTASSIUM CITRATE15 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
72162-1759-172162175901100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1759-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6271d84e-d991-4bb8-ac9f-6d5cc879b631

Use it

Look up 72162-1759 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72162-1759 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72162-1759. 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.