NDC 63323-261

Progesterone 50 mg per 1 mL injection, solution

On the label: Fresenius Kabi, LLC.

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Fresenius Kabi USA, LLCMelrose Park, IL, United StatesMakes it Problems found, fixed voluntarilyAug 24, 2023 · 13 inspections, 2 with FDA action

Product details

Generic drug
Progesterone: every company that makes it
Form
injection, solution, intramuscular
Strength
50 mg per 1 mL
Approval
ANDA ANDA075906
On the market since
Jul 19, 2001
Package NDCs
63323-261-10
Official label
DailyMed (National Library of Medicine), updated Oct 15, 2024

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