NDC 45865-356

Gabapentin 600 mg tablet

On the label: Medsource Pharmaceuticals. It's repackaged: Medsource Pharmaceuticals rebottles it from Glenmark Pharmaceuticals Inc., USA's NDC 68462-126.

India: 2United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Appco Pharma LLCPiscataway, NJ, United StatesMakes it and tests it Problems found, fixed voluntarilyMay 14, 2026 · 9 inspections
Glenmark Pharmaceuticals LimitedGoa, IndiaMakes it and tests it Problems found, fixed voluntarilyJun 30, 2026 · 7 inspections, 1 with FDA action
Glenmark Pharmaceuticals LimitedDhar, IndiaMakes it and tests it Serious problems, FDA actionFeb 14, 2025 · 8 inspections, 1 with FDA action

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
Gabapentin: every company that makes it
Form
tablet
Strength
600 mg
Approval
ANDA ANDA077662
On the market since
Apr 1, 2006
Package NDCs
45865-356-30 45865-356-49 45865-356-51 45865-356-60 45865-356-90
Official label
DailyMed (National Library of Medicine), updated Nov 10, 2019

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