Danazol - 0555-0635-09 - (Danazol)

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Drug Information of Danazol

Product NDC: 0555-0635
Proprietary Name: Danazol
Non Proprietary Name: Danazol
Active Ingredient(s): 200    mg/1 & nbsp;   Danazol
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Danazol

Product NDC: 0555-0635
Labeler Name: Barr Laboratories Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074582
Marketing Category: ANDA
Start Marketing Date: 19960809

Package Information of Danazol

Package NDC: 0555-0635-09
Package Description: 60 CAPSULE in 1 BOTTLE (0555-0635-09)

NDC Information of Danazol

NDC Code 0555-0635-09
Proprietary Name Danazol
Package Description 60 CAPSULE in 1 BOTTLE (0555-0635-09)
Product NDC 0555-0635
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Danazol
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19960809
Marketing Category Name ANDA
Labeler Name Barr Laboratories Inc.
Substance Name DANAZOL
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Androgen [EPC],Androgen Receptor Agonists [MoA],Androstanes [Chemical/Ingredient]

Complete Information of Danazol


General Information