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phenylephrine hydrochloride

NDC 36000-358, phenylephrine hydrochloride, injection, from Baxter Healthcare Corporation.

Product NDC
36000-358
Status
Listed
Labeler
Baxter Healthcare Corporation
Dosage form
INJECTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA217032
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/36000-358 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PHENYLEPHRINE HYDROCHLORIDE10 mg/mL

Pharmacologic classes

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

Package NDCNDC-11Package
36000-358-253600003582525 VIAL, SINGLE-DOSE in 1 CARTON (36000-358-25) / 1 mL in 1 VIAL, SINGLE-DOSE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/74192a42-0ff7-443b-9d8a-3096ef5c8e43

Use it

Look up 36000-358 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/36000-358 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 36000-358. 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.