REGLAN Detail

Drug Name(s):
REGLAN

FDA Application No.:
NDA 017862

Active Ingredient(s):
METOCLOPRAMIDE HYDROCHLORIDE

Company:
BAXTER HLTHCARE CORP

Original Approval or Tentative Approval Date:
February 6, 1979

Products on Application NDA 017862:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
METOCLOPRAMIDE HYDROCHLORIDE	EQ 10MG BASE/ML	INJECTABLE; INJECTION	Discontinued	none

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last updated on 11-21-2008

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