NDC 50436-0126

Gabapentin 600 mg tablet

On the label: Unit Dose Services. It's a repackaged product: Unit Dose Services rebottles it from Glenmark Pharmaceuticals Inc., USA's NDC 68462-126.

Where the pills inside were made

Piscataway, NJ, United States · makes it and tests it

Problems found, fixed voluntarily Last FDA inspection May 14, 2026. 9 inspections on record.

Goa, India · makes it and tests it

Problems found, fixed voluntarily Last FDA inspection Jun 30, 2026. 7 inspections on record, 1 with serious problems.

Dhar, India · makes it and tests it

Serious problems, FDA action Last FDA inspection Feb 14, 2025. 8 inspections on record, 1 with serious problems.

Mar 13, 2025 · Class II · Ongoing
CGMP Deviations
Lots: Lot # 17231015, exp. date Apr-25 17231128, exp. date Apr-25 17231138, exp. date Apr-25 17231139, exp. date Apr-25 17231143, exp. date Apr-25 17231144, exp. date Apr-25 17231848, exp. date Aug-25 17231898, exp. date Aug-25 17231977, exp. date Aug-25 17231978, exp. date Aug-25 17232015, exp. date Aug…
Apr 5, 2013 · Class III · Terminated
Chemical Contamination: Gabapentin Sodium tablets is recalled due to complaints related to an off - odor described as moldy, musty or fishy in nature.
Lots: a) 600mg: Lot# 02123419, Exp 10/14 Lot# 02123424, Exp 10/14 Lot# 02123430, Exp 10/14 Lot# 02123492, Exp 10/14 Lot# 02123523, Exp 10/14 Lot# 02123527, Exp 10/14 Lot# 02123532, Exp 10/14 Lot# 02123542, Exp 10/14 Lot# 02123546, Exp 10/14 Lot# 02123551, Exp 10/14 Lot# 02123555, Exp 10/14…

Generic drug: Gabapentin: see every company that makes it
Form: tablet
Strength: 600 mg
Approval: ANDA ANDA077662
On the market since: Apr 1, 2006
Package NDCs: 50436-0126-1 50436-0126-2 50436-0126-3
Official label: DailyMed (National Library of Medicine), updated Oct 11, 2017

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