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Mannitol

NDC 63323-024, MANNITOL, injection, solution, from Fresenius Kabi USA, LLC.

Product NDC
63323-024
Status
Listed
Labeler
Fresenius Kabi USA, LLC
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA080677
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/63323-024 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MANNITOL250 mg/mL

Pharmacologic classes

Increased Diuresis [PE]; Osmotic Activity [MoA]; Osmotic Diuretic [EPC]

Package NDCNDC-11Package
63323-024-256332300242525 VIAL, SINGLE-DOSE in 1 TRAY (63323-024-25) / 50 mL in 1 VIAL, SINGLE-DOSE (63323-024-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c395e13d-6ea1-4104-8b37-669cfb982f04

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=63323-024

Use it

Look up 63323-024 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63323-024 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63323-024. 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.