NDC 13533-613

Plasmanate 2.5 g per 50 mL solution

On the label: Grifols Usa, LLC.

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Grifols Therapeutics LLCClayton, NC, United StatesMakes it Not inspected on record
Grifols Worldwide Operations LimitedClondalkin, IrelandPackages it and labels it Not inspected on record

Product details

Generic drug
Albumin Human: every company that makes it
Form
solution, intravenous
Strength
2.5 g per 50 mL
Approval
BLA BLA101140
On the market since
Oct 2, 1958
Package NDCs
13533-613-25 13533-613-26
Official label
DailyMed (National Library of Medicine), updated Nov 1, 2026

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