NALOXONE HYDROCHLORIDE AND PENTAZOCAINE Detail

Drug Name(s):
NALOXONE HYDROCHLORIDE AND PENTAZOCAINE

FDA Application No.:
NDA 075735

Active Ingredient(s):
NALOXONE HYDROCHLORIDE; PENTAZOCINE HYDROCHLORIDE

Company:
ACTAVIS TOTOWA

Original Approval or Tentative Approval Date:
July 10, 2001

Products on Application NDA 075735:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
NALOXONE HYDROCHLORIDE; PENTAZOCINE HYDROCHLORIDE	EQ 0.5MG BASE;EQ 50MG BASE	TABLET; ORAL	Prescription	AB

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last updated on 12-05-2008

NALOXONE HYDROCHLORIDE AND PENTAZOCAINE Detail

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