GABAPENTIN Detail

Drug Name(s):
GABAPENTIN

FDA Application No.:
NDA 075694

Active Ingredient(s):
GABAPENTIN

Company:
ACTAVIS ELIZABETH

Products on Application NDA 075694:

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

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last updated on 01-07-2009

GABAPENTIN Detail

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