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ALBUTEIN

NDC 68516-5214, ALBUMIN (HUMAN), injection, solution, from GRIFOLS USA, LLC.

Product NDC
68516-5214
Status
Listed
Labeler
GRIFOLS USA, LLC
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Product type
PLASMA DERIVATIVE
Marketing category
BLA
Application
BLA102478
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68516-5214 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ALBUMIN HUMAN12.5 g/250mL

Pharmacologic classes

Human Serum Albumin [EPC]; Increased Intravascular Volume [PE]; Increased Oncotic Pressure [PE]; Osmotic Activity [MoA]; Serum Albumin [Chemical/Ingredient]

Package NDCNDC-11Package
68516-5214-1685165214011 VIAL in 1 CARTON (68516-5214-1) / 250 mL in 1 VIAL (68516-5214-3)
68516-5214-2685165214021 VIAL in 1 CARTON (68516-5214-2) / 500 mL in 1 VIAL (68516-5214-4)
68516-5214-5685165214051 VIAL in 1 CARTON (68516-5214-5) / 50 mL in 1 VIAL (68516-5214-6)

Linked data

RxNorm, label and prices

Use it

Look up 68516-5214 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68516-5214 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68516-5214. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.