Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 075406

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OGESTREL 0.5/50-21 (ETHINYL ESTRADIOL; NORGESTREL)
0.05MG;0.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued

Active Ingredient: ETHINYL ESTRADIOL; NORGESTREL
Proprietary Name: OGESTREL 0.5/50-21
Dosage Form; Route of Administration: TABLET; ORAL-21
Strength: 0.05MG;0.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A075406
Product Number: 001
Approval Date: Dec 15, 1999
Applicant Holder Full Name: WATSON LABORATORIES INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

OGESTREL 0.5/50-28 (ETHINYL ESTRADIOL; NORGESTREL)
0.05MG;0.5MG
Marketing Status: Discontinued

Active Ingredient: ETHINYL ESTRADIOL; NORGESTREL
Proprietary Name: OGESTREL 0.5/50-28
Dosage Form; Route of Administration: TABLET; ORAL-28
Strength: 0.05MG;0.5MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A075406
Product Number: 002
Approval Date: Dec 15, 1999
Applicant Holder Full Name: WATSON LABORATORIES INC
Marketing Status:  Discontinued
Patent and Exclusivity Information