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Sodium Citrate and Citric Acid

NDC 60687-832, SODIUM CITRATE and CITRIC ACID MONOHYDRATE, solution, from American Health Packaging.

Product NDC
60687-832
Status
Listed
Labeler
American Health Packaging
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/60687-832 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM CITRATE, UNSPECIFIED FORM1500 mg/15mL
  • ANHYDROUS CITRIC ACID1002 mg/15mL

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
60687-832-166068708321610 TRAY in 1 CASE (60687-832-16) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-832-50) / 15 mL in 1 CUP, UNIT-DOSE (60687-832-44)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/58fa9952-c8ab-4ebb-a073-15cc45f4832a

Use it

Look up 60687-832 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/60687-832 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 60687-832. 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.