Last Updated: November 13, 2026

Details for New Drug Application (NDA): 075350

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NDA 075350 describes GABAPENTIN, which is a drug marketed by Actavis Elizabeth, Alkem, Amneal Pharms Ny, Ascent Pharms Inc, Aurobindo Pharma, Chartwell Rx, Cspc Ouyi, Granules, Hikma, Invagen Pharms, Ipca Labs Ltd, Pharmazone, Pharmobedient, Prinston Inc, Rising, Sandoz, Strides Pharma, Sun Pharm Inds Ltd, Sun Pharm Industries, Taro, Teva Pharms, Watson Labs, Zhejiang Yongtai, Acella Pharms Llc, Ajenat Pharms, Amneal Pharms, Annora Pharma, Mission Pharmacal, Pai Holdings Pharm, Rubicon Research, Abon Pharms Llc, Alkem Labs Ltd, Apotex, Aurobindo Pharma Ltd, Epic Pharma Llc, Glenmark Pharms Ltd, Hikma Pharms, Ivax Sub Teva Pharms, Lupin, Ranbaxy, Sciegen Pharms, Teva, Teva Pharms Usa, Zydus Pharms, and Zydus Pharms Usa Inc, and is included in sixty-nine NDAs. It is available from eighty-three suppliers. Additional details are available on the GABAPENTIN profile page.

The generic ingredient in GABAPENTIN is gabapentin. There is one drug master file entry for this compound. Ninety suppliers are listed for this compound. Additional details are available on the gabapentin profile page.

Summary for 075350

Tradename:	GABAPENTIN
Applicant:	Actavis Elizabeth
Ingredient:	gabapentin
Patents:	0

Pharmacology for NDA: 075350

Physiological Effect	Decreased Central Nervous System Disorganized Electrical Activity

Suppliers and Packaging for NDA: 075350

Tradename	Generic Name	Dosage	NDA	Application Type	Supplier	National Drug Code	Package Code	Package
GABAPENTIN	gabapentin	CAPSULE;ORAL	075350	ANDA	Teva Pharmaceuticals, Inc.	0480-3494	0480-3494-05	500 CAPSULE in 1 BOTTLE (0480-3494-05)
GABAPENTIN	gabapentin	CAPSULE;ORAL	075350	ANDA	Teva Pharmaceuticals, Inc.	0480-3495	0480-3495-01	100 CAPSULE in 1 BOTTLE (0480-3495-01)

Profile for product number 001

Active Rx/OTC/Discontinued:	RX	Dosage:	CAPSULE;ORAL			Strength	100MG
Approval Date:	Sep 12, 2003	TE:	AB	RLD:	No

Profile for product number 002

Active Rx/OTC/Discontinued:	RX	Dosage:	CAPSULE;ORAL			Strength	300MG
Approval Date:	Sep 12, 2003	TE:	AB	RLD:	No

Profile for product number 003

Active Rx/OTC/Discontinued:	RX	Dosage:	CAPSULE;ORAL			Strength	400MG
Approval Date:	Sep 12, 2003	TE:	AB	RLD:	No

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