Danazol - 0527-1369-01 - (Danazol)

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Drug Information of Danazol

Product NDC: 0527-1369
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: 0527-1369
Labeler Name: Lannett Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077246
Marketing Category: ANDA
Start Marketing Date: 20050928

Package Information of Danazol

Package NDC: 0527-1369-01
Package Description: 100 CAPSULE in 1 BOTTLE (0527-1369-01)

NDC Information of Danazol

NDC Code 0527-1369-01
Proprietary Name Danazol
Package Description 100 CAPSULE in 1 BOTTLE (0527-1369-01)
Product NDC 0527-1369
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Danazol
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20050928
Marketing Category Name ANDA
Labeler Name Lannett Company, 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