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PHENYLEPHRINE HYDROCHLORIDE

NDC 70069-802, PHENYLEPHRINE HYDROCHLORIDE, injection, from Somerset Therapeutics, LLC.

Product NDC
70069-802
Status
Listed
Labeler
Somerset Therapeutics, LLC
Dosage form
INJECTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213318
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70069-802 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PHENYLEPHRINE HYDROCHLORIDE50 mg/5mL

Pharmacologic classes

Adrenergic alpha1-Agonists [MoA]; alpha-1 Adrenergic Agonist [EPC]

Package NDCNDC-11Package
70069-802-107006908021010 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (70069-802-10) / 5 mL in 1 VIAL, PHARMACY BULK PACKAGE (70069-802-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/90a3853e-49d6-4536-be72-82cc875bcf74

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=70069-802

Use it

Look up 70069-802 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70069-802 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70069-802. 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.