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Prochlorperazine Edisylate

NDC 0713-0351, Prochlorperazine Edisylate, injection, from Cosette Pharmaceuticals, Inc..

Product NDC
0713-0351
Status
Listed
Labeler
Cosette Pharmaceuticals, Inc.
Dosage form
INJECTION
Route
INTRAMUSCULAR, INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213626
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0713-0351 \
  -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
0713-0351-090071303510910 VIAL in 1 PACKAGE (0713-0351-09) / 2 mL in 1 VIAL (0713-0351-02)
0713-0351-250071303512525 VIAL in 1 PACKAGE (0713-0351-25) / 2 mL in 1 VIAL (0713-0351-02)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4687b9f5-2d67-4fe0-af4d-2415a42b5292

Use it

Look up 0713-0351 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0713-0351 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0713-0351. 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.