NDC 63187-010

Gabapentin 800 mg tablet

On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP 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

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, oral
Strength
800 mg
Approval
ANDA ANDA077662
On the market since
Apr 1, 2006
Package NDCs
63187-010-30 63187-010-60 63187-010-90
Official label
DailyMed (National Library of Medicine), updated Oct 1, 2019

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