NDC 76420-059

Progesterone 200 mg capsule

On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Amneal Pharmaceuticals's NDC 65162-808.

United States: 1

Where the pills inside were 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

Repackaging site

Product details

Generic drug
Progesterone: every company that makes it
Form
capsule, oral
Strength
200 mg
Approval
ANDA ANDA207724
On the market since
Sep 11, 2017
Package NDCs
76420-059-10 76420-059-30 76420-059-90
Official label
DailyMed (National Library of Medicine), updated Oct 12, 2022

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