NATURETIN-2.5 Detail

Drug Name(s):
NATURETIN-2.5

FDA Application No.:
NDA 012164

Active Ingredient(s):
BENDROFLUMETHIAZIDE

Company:
APOTHECON

Original Approval or Tentative Approval Date:
December 28, 1976

Products on Application NDA 012164:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
BENDROFLUMETHIAZIDE	10MG	TABLET; ORAL	Discontinued	none
BENDROFLUMETHIAZIDE	2.5MG	TABLET; ORAL	Discontinued	none

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last updated on 11-21-2008

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