NDC 0406-8320

Morphine Sulfate 200 mg tablet, extended release

On the label: SpecGx LLC.

United States: 2

Where it's made

FactoryWhereRoleLast FDA inspection
SpecGx LLCHobart, NY, United StatesMakes it and tests it No problems foundMar 13, 2020 · 6 inspections
SpecGx LLCSt. Louis, MO, United StatesMakes the active ingredient Problems found, fixed voluntarilyOct 22, 2025 · 8 inspections

Product details

Generic drug
Morphine: every company that makes it
Form
tablet, extended release, oral
Strength
200 mg
Approval
ANDA ANDA076438
On the market since
Jul 3, 2003
Package NDCs
0406-8320-01
Official label
DailyMed (National Library of Medicine), updated Aug 27, 2026

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