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Prochlorperazine Edisylate

NDC 68083-435, Prochlorperazine Edisylate, injection, from Gland Pharma Limited.

Product NDC
68083-435
Status
Listed
Labeler
Gland Pharma Limited
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/68083-435 \
  -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
68083-435-106808304351010 VIAL in 1 CARTON (68083-435-10) / 2 mL in 1 VIAL (68083-435-01)
68083-435-256808304352525 VIAL in 1 CARTON (68083-435-25) / 2 mL in 1 VIAL (68083-435-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a0fd3d58-7470-4d0f-9e6c-84e92c02a97f

Use it

Look up 68083-435 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68083-435 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68083-435. 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.