NDC 65162-778

Budesonide 3 mg capsule, delayed release

On the label: Amneal Pharmaceuticals.

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Amneal Pharmaceuticals of New York, LLCBrookhaven, NY, United StatesMakes it, tests it, packages it and labels it No problems foundSep 25, 2026 · 14 inspections

Product details

Generic drug
Budesonide: every company that makes it
Form
capsule, delayed release, oral
Strength
3 mg
Approval
ANDA ANDA206200
On the market since
Sep 15, 2017
Package NDCs
65162-778-10 65162-778-18 65162-778-30 65162-778-49
Official label
DailyMed (National Library of Medicine), updated Sep 19, 2024

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