GABAPENTIN Detail

Drug Name(s):
GABAPENTIN

FDA Application No.:
NDA 076120

Active Ingredient(s):
GABAPENTIN

Company:
SANDOZ

Original Approval or Tentative Approval Date:
January 26, 2006

Products on Application NDA 076120:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
GABAPENTIN	800MG	TABLET; ORAL	Prescription	AB

Recall Notices

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FDA Announces Class I Recall of Ophthalmic Surgical Device
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KRC Food Trading Inc. Recall of Fish Cake Sushi (December 23)

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January 2009

GABAPENTIN Detail

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