UROCIT-K Detail

Drug Name(s):
UROCIT-K

FDA Application No.:
NDA 019071

Active Ingredient(s):
POTASSIUM CITRATE

Company:
MISSION PHARMA

Original Approval or Tentative Approval Date:
August 29, 1985

Products on Application NDA 019071:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
POTASSIUM CITRATE	10MEQ	TABLET, EXTENDED RELEASE; ORAL	Prescription	AB

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last updated on 11-21-2008

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