NDC 64725-0126

Gabapentin 600 mg tablet

On the label: TYA Pharmaceuticals. It's repackaged: TYA 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
64725-0126-1
Official label
DailyMed (National Library of Medicine), updated Jun 30, 2013

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