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Last Updated: April 23, 2024

Details for New Drug Application (NDA): 021319


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NDA 021319 describes AVODART, which is a drug marketed by Woodward and is included in one NDA. It is available from one supplier. Additional details are available on the AVODART profile page.

The generic ingredient in AVODART is dutasteride. There are eighteen drug master file entries for this compound. Seventeen suppliers are listed for this compound. Additional details are available on the dutasteride profile page.
Summary for 021319
Tradename:AVODART
Applicant:Woodward
Ingredient:dutasteride
Patents:0
Formulation / Manufacturing:see details
Pharmacology for NDA: 021319
Mechanism of Action5-alpha Reductase Inhibitors
Medical Subject Heading (MeSH) Categories for 021319
Suppliers and Packaging for NDA: 021319
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
AVODART dutasteride CAPSULE;ORAL 021319 NDA Waylis Therapeutics LLC 80725-712 80725-712-04 90 CAPSULE, LIQUID FILLED in 1 BOTTLE (80725-712-04)
AVODART dutasteride CAPSULE;ORAL 021319 NDA Waylis Therapeutics LLC 80725-712 80725-712-15 30 CAPSULE, LIQUID FILLED in 1 BOTTLE (80725-712-15)

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:CAPSULE;ORALStrength0.5MG
Approval Date:Nov 20, 2001TE:ABRLD:Yes

Expired US Patents for NDA 021319

Applicant Tradename Generic Name Dosage NDA Approval Date Patent No. Patent Expiration
Woodward AVODART dutasteride CAPSULE;ORAL 021319-001 Nov 20, 2001 ⤷  Try a Trial ⤷  Try a Trial
Woodward AVODART dutasteride CAPSULE;ORAL 021319-001 Nov 20, 2001 ⤷  Try a Trial ⤷  Try a Trial
Woodward AVODART dutasteride CAPSULE;ORAL 021319-001 Nov 20, 2001 ⤷  Try a Trial ⤷  Try a Trial
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >Patent No. >Patent Expiration

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