NDC 70121-1685

Exenatide 250 ug per 1 mL injection

On the label: Amneal Pharmaceuticals LLC.

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Amneal Pharmaceuticals Private LimitedAhmedabad, IndiaMakes it, tests it, packages it and sterilizes it No problems foundJun 19, 2024 · 7 inspections

Recalls

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug
Exenatide: every company that makes it
Form
injection, subcutaneous
Strength
250 ug per 1 mL
Approval
ANDA ANDA206697
On the market since
Nov 22, 2024
Package NDCs
70121-1685-1
Official label
DailyMed (National Library of Medicine), updated May 27, 2026

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