NDC 68071-3967

Spironolactone 25 mg tablet, coated

On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Oxford Pharmaceuticals, LLC's NDC 69584-852.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Oxford Pharmaceuticals, LLCBirmingham, AL, United StatesMakes it Problems found, fixed voluntarilyNov 3, 2023 · 3 inspections

Repackaging site

Product details

Generic drug
Spironolactone: every company that makes it
Form
tablet, coated, oral
Strength
25 mg
Approval
ANDA ANDA040750
On the market since
Jan 4, 2021
Package NDCs
68071-3967-3
Official label
DailyMed (National Library of Medicine), updated Feb 20, 2026

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