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POTASSIUM CITRATE

NDC 70518-4477, Potassium Citrate, tablet, extended release, from REMEDYREPACK INC..

Product NDC
70518-4477
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA214420
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4477 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • POTASSIUM CITRATE10 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
70518-4477-070518447700100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4477-0)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/08c769d4-1dc0-4130-8f9c-cddace13a79b

Use it

Look up 70518-4477 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4477 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-4477. 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.