NDC 59088-178

Pretrate 20 ingredients tablet

On the label: PureTek Corporation.

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
PureTek CorporationSan Fernando, CA, United StatesMakes it, packages it and labels it Problems found, fixed voluntarilyMar 7, 2025 · 10 inspections

Product details

Generic drug
Ferrous Fumarate, Folic Acid: every company that makes it
Form
tablet, oral
Strength
20 ingredients
Approval
unapproved drug other
On the market since
Feb 1, 2021
Package NDCs
59088-178-54
Official label
DailyMed (National Library of Medicine), updated Sep 30, 2024

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