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Prochlorperazine Edisylate

NDC 0641-6135, Prochlorperazine Edisylate, injection, from Hikma Pharmaceuticals USA Inc..

Product NDC
0641-6135
Status
Listed
Labeler
Hikma Pharmaceuticals USA Inc.
Dosage form
INJECTION
Route
INTRAMUSCULAR, INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA089903
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0641-6135 \
  -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
0641-6135-250064161352525 VIAL in 1 CARTON (0641-6135-25) / 2 mL in 1 VIAL (0641-6135-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/baf59816-7577-4652-b065-fb6de9e54569

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=0641-6135

Use it

Look up 0641-6135 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0641-6135 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0641-6135. 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.