NDC 61916-090

Drospirenone and Ethinyl Estradiol 3 mg / 0.02 mg kit

On the label: Pharmaceutics International, Inc. (Pii).

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Pharmaceutics International, Inc.Hunt Valley, MD, United StatesMakes it and tests it Problems found, fixed voluntarilyDec 6, 2024 · 14 inspections

Product details

Generic drug
Drospirenone and Ethinyl Estradiol: every company that makes it
Form
kit
Strength
3 mg / 0.02 mg
Approval
ANDA ANDA203291
On the market since
Oct 26, 2017
Package NDCs
61916-090-30
Official label
DailyMed (National Library of Medicine), updated Jul 26, 2017

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