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PROCHLORPERAZINE EDISYLATE

NDC 43066-090, prochlorperazine edisylate, injection, from Baxter Healthcare Corporation.

Product NDC
43066-090
Status
Listed
Labeler
Baxter Healthcare Corporation
Dosage form
INJECTION
Route
INTRAMUSCULAR, INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA214379
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/43066-090 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PROCHLORPERAZINE EDISYLATE5 mg/mL

Pharmacologic classes

Phenothiazine [EPC]; Phenothiazines [CS]

Package NDCNDC-11Package
43066-090-254306600902525 VIAL in 1 CARTON (43066-090-25) / 2 mL in 1 VIAL (43066-090-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/11cb37c7-01b4-4223-b2ea-a3695639b80b

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=43066-090

Use it

Look up 43066-090 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/43066-090 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 43066-090. 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.