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Hydromorphone Hydrochloride

NDC 63323-854, Hydromorphone Hydrochloride, injection, solution, from Fresenius Kabi USA, LLC.

Product NDC
63323-854
Status
Listed
Labeler
Fresenius Kabi USA, LLC
Dosage form
INJECTION, SOLUTION
Route
INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA019034
DEA schedule
CII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/63323-854 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • HYDROMORPHONE HYDROCHLORIDE4 mg/mL

Pharmacologic classes

Full Opioid Agonists [MoA]; Opioid Agonist [EPC]

Package NDCNDC-11Package
63323-854-106332308541025 VIAL, SINGLE-DOSE in 1 CARTON (63323-854-10) / 1 mL in 1 VIAL, SINGLE-DOSE (63323-854-03)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e034eb96-03e0-46e1-8b92-5e1f94555e7b

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=63323-854

Use it

Look up 63323-854 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63323-854 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63323-854. 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.