Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

Home | Back to Search Results

Product Details for ANDA 075256

Expand all

DESOGESTREL AND ETHINYL ESTRADIOL (DESOGESTREL; ETHINYL ESTRADIOL)
0.15MG;0.03MG
Marketing Status: Prescription

Active Ingredient: DESOGESTREL; ETHINYL ESTRADIOL
Proprietary Name: DESOGESTREL AND ETHINYL ESTRADIOL
Dosage Form; Route of Administration: TABLET; ORAL-28
Strength: 0.15MG;0.03MG
Reference Listed Drug: No
Reference Standard: Yes
TE Code: AB
Application Number: A075256
Product Number: 002
Approval Date: Aug 12, 1999
Applicant Holder Full Name: DURAMED PHARMACEUTICALS INC SUB BARR LABORATORIES INC
Marketing Status:  Prescription
Patent and Exclusivity Information

DESOGESTREL AND ETHINYL ESTRADIOL (DESOGESTREL; ETHINYL ESTRADIOL)
0.15MG;0.03MG
Marketing Status: Discontinued

Active Ingredient: DESOGESTREL; ETHINYL ESTRADIOL
Proprietary Name: DESOGESTREL AND ETHINYL ESTRADIOL
Dosage Form; Route of Administration: TABLET; ORAL-21
Strength: 0.15MG;0.03MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A075256
Product Number: 001
Approval Date: Aug 12, 1999
Applicant Holder Full Name: DURAMED PHARMACEUTICALS INC SUB BARR LABORATORIES INC
Marketing Status:  Discontinued
Patent and Exclusivity Information