NDC 52246-570

Spinosad 9 mg per 1 mL suspension

On the label: ParaPRO LLC.

United States: 2

Where it's made

FactoryWhereRoleLast FDA inspection
Ferndale Laboratories, Inc.Ferndale, MI, United StatesMakes it and packages it Problems found, fixed voluntarilyFeb 27, 2026 · 10 inspections, 2 with FDA action
Pharmaceutics International, Inc.Hunt Valley, MD, United StatesMakes it and packages it Problems found, fixed voluntarilyDec 6, 2024 · 14 inspections

Product details

Generic drug
Spinosad: every company that makes it
Form
suspension, topical
Strength
9 mg per 1 mL
Approval
NDA authorized generic NDA022408
On the market since
Jan 29, 2024
Package NDCs
52246-570-04
Official label
DailyMed (National Library of Medicine), updated Jan 29, 2024

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