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Sodium Citrate and Citric Acid

NDC 0121-1190, SODIUM CITRATE and CITRIC ACID MONOHYDRATE, solution, from Pharmaceutical Associates, Inc..

Product NDC
0121-1190
Status
Listed
Labeler
Pharmaceutical Associates, Inc.
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/0121-1190 \
  -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
0121-1190-000012111900010 TRAY in 1 CASE (0121-1190-00) / 10 CUP, UNIT-DOSE in 1 TRAY / 30 mL in 1 CUP, UNIT-DOSE (0121-1190-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/63201a61-6ac5-41ae-8b2d-ff0d3a8ddfd5

Use it

Look up 0121-1190 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0121-1190 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0121-1190. 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.