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NDC 76125-791, Albumin (Human), solution, from KEDRION BIOPHARMA, INC..

Product NDC
76125-791
Status
Listed
Labeler
KEDRION BIOPHARMA, INC.
Dosage form
SOLUTION
Route
INTRAVENOUS
Product type
PLASMA DERIVATIVE
Marketing category
BLA
Application
BLA101138
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/76125-791 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ALBUMIN HUMAN10 g/50mL

Pharmacologic classes

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

Package NDCNDC-11Package
76125-791-10761250791101 VIAL in 1 CARTON (76125-791-10) / 100 mL in 1 VIAL (76125-791-11)
76125-791-50761250791501 VIAL in 1 CARTON (76125-791-50) / 50 mL in 1 VIAL (76125-791-51)

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 76125-791 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/76125-791 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 76125-791. 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.