REGLAN Detail

Drug Name(s):
REGLAN

FDA Application No.:
NDA 017854

Active Ingredient(s):
METOCLOPRAMIDE HYDROCHLORIDE

Company:
SCHWARZ PHARMA

Original Approval or Tentative Approval Date:
December 29, 1980

Products on Application NDA 017854:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
METOCLOPRAMIDE HYDROCHLORIDE	EQ 10MG BASE	TABLET; ORAL	Prescription	AB

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last updated on 11-21-2008

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