NDC 0069-1306

Retacrit 3000 [iU] per 1 mL injection, solution

On the label: Pfizer Laboratories Div Pfizer Inc.

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Hospira, Inc.McPherson, KS, United StatesMakes it, tests it, packages it and labels it Problems found, fixed voluntarilyJan 17, 2025 · 16 inspections, 2 with FDA action
Eurofins BioPharma Product Testing Leiden B.V.Leiden, NetherlandsTests it Problems found, fixed voluntarilyJul 1, 2022 · 5 inspections

Product details

Generic drug
Erythropoietin: every company that makes it
Form
injection, solution, intravenous; subcutaneous
Strength
3000 [iU] per 1 mL
Approval
BLA BLA125545
On the market since
Jun 18, 2018
Package NDCs
0069-1306-01 0069-1306-10
Official label
DailyMed (National Library of Medicine), updated Jun 22, 2025

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