M-ZOLE 7 DUAL PACK Detail

Drug Name(s):
M-ZOLE 7 DUAL PACK

FDA Application No.:
NDA 074586

Active Ingredient(s):
MICONAZOLE NITRATE

Company:
ACTAVIS MID ATLANTIC

Original Approval or Tentative Approval Date:
September 30, 1998

Products on Application NDA 074586:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
MICONAZOLE NITRATE	2%,100MG	CREAM, SUPPOSITORY; TOPICAL, VAGINAL	OTC	none

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last updated on 12-01-2008