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Potassium Citrate

NDC 70518-3160, Potassium Citrate, tablet, extended release, from REMEDYREPACK INC..

Product NDC
70518-3160
Status
Listed
Labeler
REMEDYREPACK INC.
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/70518-3160 \
  -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
70518-3160-070518316000100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-3160-0)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a9cc636d-3e26-450c-9df8-665d530d626f

Use it

Look up 70518-3160 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3160 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-3160. 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.