Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 010611

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HALOTESTIN (FLUOXYMESTERONE)
2MG
Marketing Status: Discontinued

Active Ingredient: FLUOXYMESTERONE
Proprietary Name: HALOTESTIN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 2MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N010611
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PHARMACIA AND UPJOHN CO
Marketing Status:  Discontinued
Patent and Exclusivity Information

HALOTESTIN (FLUOXYMESTERONE)
5MG
Marketing Status: Discontinued

Active Ingredient: FLUOXYMESTERONE
Proprietary Name: HALOTESTIN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 5MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N010611
Product Number: 006
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PHARMACIA AND UPJOHN CO
Marketing Status:  Discontinued
Patent and Exclusivity Information

HALOTESTIN (FLUOXYMESTERONE)
10MG
Marketing Status: Discontinued

Active Ingredient: FLUOXYMESTERONE
Proprietary Name: HALOTESTIN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 10MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N010611
Product Number: 010
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PHARMACIA AND UPJOHN CO
Marketing Status:  Discontinued
Patent and Exclusivity Information