JUNEL FE 1/20 Detail

Drug Name(s):
JUNEL FE 1/20

FDA Application No.:
NDA 076081

Active Ingredient(s):
ETHINYL ESTRADIOL; NORETHINDRONE ACETATE

Company:
BARR

Original Approval or Tentative Approval Date:
September 17, 2003

Products on Application NDA 076081:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
ETHINYL ESTRADIOL; NORETHINDRONE ACETATE	0.02MG;1MG	TABLET; ORAL-28	Prescription	AB

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last updated on 11-19-2008

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