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Sodium Citrate and Citric Acid

NDC 17856-0595, SODIUM CITRATE and CITRIC ACID MONOHYDRATE, solution, from Atlantic Biologicals Corp..

Product NDC
17856-0595
Status
Listed
Labeler
Atlantic Biologicals Corp.
Dosage form
SOLUTION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
UNAPPROVED DRUG OTHER
Application
—
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/17856-0595 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM CITRATE500 mg/5mL
  • ANHYDROUS CITRIC ACID334 mg/5mL

Pharmacologic classes

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

Package NDCNDC-11Package
17856-0595-11785605950172 CUP, UNIT-DOSE in 1 CASE (17856-0595-1) / 15 mL in 1 CUP, UNIT-DOSE
17856-0595-31785605950350 CUP in 1 CASE (17856-0595-3) / 30 mL in 1 CUP

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/42d837ae-2578-46df-92d2-24774964aaad

Use it

Look up 17856-0595 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/17856-0595 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 17856-0595. 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.