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ALBUTEIN

NDC 68516-5219, ALBUMIN (HUMAN), injection, solution, from GRIFOLS USA, LLC.

Product NDC
68516-5219
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/68516-5219 \
  -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
68516-5219-1685165219011 BAG in 1 CARTON (68516-5219-1) / 500 mL in 1 BAG (68516-5219-0)
68516-5219-2685165219022 BAG in 1 CARTON (68516-5219-2) / 500 mL in 1 BAG (68516-5219-0)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.

Use it

Look up 68516-5219 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68516-5219 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68516-5219. 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.