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Prochlorperazine Edisylate

NDC 70069-371, Prochlorperazine Edisylate, injection, from Somerset Therapeutics, LLC.

Product NDC
70069-371
Status
Listed
Labeler
Somerset Therapeutics, LLC
Dosage form
INJECTION
Route
INTRAMUSCULAR, INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA212257
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70069-371 \
  -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
70069-371-257006903712525 VIAL in 1 CARTON (70069-371-25) / 2 mL in 1 VIAL (70069-371-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d382e3d4-3175-42f2-b9eb-d9a7b97cbbfc

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=70069-371

Use it

Look up 70069-371 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70069-371 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70069-371. 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.