NDC 52959-772

Gabapentin 800 mg tablet

On the label: H.J. Harkins Co., Inc.. It's repackaged: H.J. Harkins Co., Inc. rebottles it from Glenmark Pharmaceuticals Inc., USA's NDC 68462-127.

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

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
800 mg
Approval
ANDA ANDA077662
On the market since
Apr 1, 2006
Package NDCs
52959-772-02 52959-772-30 52959-772-60 52959-772-90
Official label
DailyMed (National Library of Medicine), updated Apr 18, 2012

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