NDC 0603-2115

Allopurinol 100 mg tablet

On the label: ENDO USA, Inc..

United States: 1India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
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
Generics Bidco II LLC d/b/a Prinston LaboratoriesCharlotte, NC, United StatesPackages it and labels it Problems found, fixed voluntarilySep 19, 2025 · 10 inspections, 1 with FDA action

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
Allopurinol: every company that makes it
Form
tablet, oral
Strength
100 mg
Approval
ANDA ANDA075798
On the market since
Jun 27, 2003
Package NDCs
0603-2115-02 0603-2115-04 0603-2115-21 0603-2115-28 0603-2115-32 0603-2115-93
Official label
DailyMed (National Library of Medicine), updated Jan 30, 2024

Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?