VELIVET Detail

Drug Name(s):
VELIVET

FDA Application No.:
NDA 076455

Active Ingredient(s):
DESOGESTREL; ETHINYL ESTRADIOL

Company:
DURAMED PHARMS BARR

Original Approval or Tentative Approval Date:
February 23, 2004

Products on Application NDA 076455:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
DESOGESTREL; ETHINYL ESTRADIOL	0.15MG/0.025MG	Tablet; Oral	Prescription	none
DESOGESTREL; ETHINYL ESTRADIOL	0.1MG,0.125MG,0.15MG;0.025MG,0.025MG,0.025MG	TABLET; ORAL-28	Prescription	AB

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last updated on 11-19-2008

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