Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
01 3SANOFI AVENTIS US
02 1AM THERAP
03 3BARR
04 2LANNETT
05 3LANNETT CO INC
01 12CAPSULE;ORAL
01 4DISCN
02 6RX
03 2Blank
01 9DANAZOL
02 3DANOCRINE
01 10No
02 2Blank
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
RLD : No
TE Code :
Brand Name : DANOCRINE
Dosage Form : CAPSULE;ORAL
Dosage Strength : 200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 17557
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
RLD : No
TE Code :
Brand Name : DANOCRINE
Dosage Form : CAPSULE;ORAL
Dosage Strength : 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 17557
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
RLD : No
TE Code :
Brand Name : DANOCRINE
Dosage Form : CAPSULE;ORAL
Dosage Strength : 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 17557
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : DANAZOL
Dosage Form : CAPSULE;ORAL
Dosage Strength : 200MG
Approval Date : 1987-12-30
Application Number : 71569
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code : AB
Brand Name : DANAZOL
Dosage Form : CAPSULE;ORAL
Dosage Strength : 200MG
Approval Date : 1996-08-09
Application Number : 74582
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : DANAZOL
Dosage Form : CAPSULE;ORAL
Dosage Strength : 100MG
Approval Date : 1998-05-29
Application Number : 74582
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : DANAZOL
Dosage Form : CAPSULE;ORAL
Dosage Strength : 50MG
Approval Date : 1998-05-29
Application Number : 74582
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : DANAZOL
Dosage Form : CAPSULE;ORAL
Dosage Strength : 200MG
Approval Date : 2005-09-28
Application Number : 77246
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : DANAZOL
Dosage Form : CAPSULE;ORAL
Dosage Strength : 50MG
Approval Date : 2007-04-19
Application Number : 77246
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : DANAZOL
Dosage Form : CAPSULE;ORAL
Dosage Strength : 100MG
Approval Date : 2007-04-19
Application Number : 77246
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
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