NDC 69367-414

Theophylline(Anhydrous) 400 mg tablet, extended release

On the label: Westminster Pharmaceuticals, LLC.

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
MPP Pharma LLCKansas City, MO, United StatesMakes it, tests it, packages it and labels it Serious problems, FDA actionApr 2, 2026 · 12 inspections, 4 with FDA action

Product details

Generic drug
Theophylline: every company that makes it
Form
tablet, extended release, oral
Strength
400 mg
Approval
ANDA ANDA040560
On the market since
Nov 25, 2025
Package NDCs
69367-414-01
Official label
DailyMed (National Library of Medicine), updated Dec 4, 2025

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