NDC 63187-037

Prednisone 10 mg tablet

On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP rebottles it from Par Health USA, LLC's NDC 0603-5338.

United States: 2India: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Generics Bidco II LLC d/b/a Prinston LaboratoriesCharlotte, NC, United StatesMakes it, packages it and labels it Problems found, fixed voluntarilySep 19, 2025 · 10 inspections, 1 with FDA action
Generics Bidco II LLC d/b/a Prinston LaboratoriesCharlotte, NC, United StatesMakes it and tests it Problems found, fixed voluntarilySep 19, 2025 · 10 inspections, 1 with FDA action
Par Formulations Private LimitedChennai, IndiaMakes it, tests it and packages it Problems found, fixed voluntarilyJun 10, 2026 · 7 inspections

Repackaging site

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
Prednisone: every company that makes it
Form
tablet, oral
Strength
10 mg
Approval
ANDA ANDA040256
On the market since
Jul 12, 2002
Package NDCs
63187-037-05 63187-037-08 63187-037-09 63187-037-10 63187-037-20 63187-037-21 63187-037-30 63187-037-40 63187-037-42
Official label
DailyMed (National Library of Medicine), updated May 1, 2021

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