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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 077246
Company: LANNETT CO INC
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
DANAZOL DANAZOL 200MG CAPSULE;ORAL Prescription AB No No
DANAZOL DANAZOL 50MG CAPSULE;ORAL Prescription AB No No
DANAZOL DANAZOL 100MG CAPSULE;ORAL Prescription AB No No
Original Approvals or Tentative Approvals
Action Date Submission Action Type Submission Classification Review Priority; Orphan Status Letters, Reviews, Labels, Patient Package Insert Notes Url
09/28/2005 ORIG-1 Approval

Label is not available on this site.

Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
08/22/2018 SUPPL-14 Labeling-Package Insert

Label is not available on this site.

03/15/2012 SUPPL-6 Labeling-Package Insert

Label is not available on this site.

10/29/2007 SUPPL-4 Labeling

Label is not available on this site.

DANAZOL

CAPSULE;ORAL; 200MG
TE Code = AB

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD TE Code Application No. Company
DANAZOL DANAZOL 200MG CAPSULE;ORAL Prescription No AB 074582 BARR
DANAZOL DANAZOL 200MG CAPSULE;ORAL Prescription No AB 077246 LANNETT CO INC

CAPSULE;ORAL; 50MG
TE Code = AB

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD TE Code Application No. Company
DANAZOL DANAZOL 50MG CAPSULE;ORAL Prescription No AB 074582 BARR
DANAZOL DANAZOL 50MG CAPSULE;ORAL Prescription No AB 078214 LANNETT
DANAZOL DANAZOL 50MG CAPSULE;ORAL Prescription No AB 077246 LANNETT CO INC

CAPSULE;ORAL; 100MG
TE Code = AB

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD TE Code Application No. Company
DANAZOL DANAZOL 100MG CAPSULE;ORAL Prescription No AB 074582 BARR
DANAZOL DANAZOL 100MG CAPSULE;ORAL Prescription No AB 078214 LANNETT
DANAZOL DANAZOL 100MG CAPSULE;ORAL Prescription No AB 077246 LANNETT CO INC
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