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POTASSIUM CITRATE

NDC 71335-2897, Potassium Citrate, tablet, extended release, from Bryant Ranch Prepack.

Product NDC
71335-2897
Status
Listed
Labeler
Bryant Ranch Prepack
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/71335-2897 \
  -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
71335-2897-171335289701100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2897-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b3ccba22-48cd-45f8-8c72-b80f34fe56be

Use it

Look up 71335-2897 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2897 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-2897. 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.