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PROCHLORPERAZINE EDISYLATE

NDC 25021-790, PROCHLORPERAZINE EDISYLATE, injection, from Sagent Pharmaceuticals.

Product NDC
25021-790
Status
Listed
Labeler
Sagent Pharmaceuticals
Dosage form
INJECTION
Route
INTRAMUSCULAR, INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA214107
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/25021-790 \
  -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
25021-790-022502107900210 VIAL in 1 CARTON (25021-790-02) / 2 mL in 1 VIAL
25021-790-032502107900325 VIAL in 1 CARTON (25021-790-03) / 2 mL in 1 VIAL

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/fed5ed29-7091-4b3c-bf67-64f32cd189bb

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=25021-790

Use it

Look up 25021-790 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/25021-790 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 25021-790. 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.