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Last Updated: January 25, 2022

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 074731

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NDA 074731 describes MINOXIDIL (FOR WOMEN), which is a drug marketed by P And L, Taro, Akorn, Apotex Inc, L Perrigo Co, and Sight Pharms, and is included in six NDAs. It is available from seventeen suppliers. Additional details are available on the MINOXIDIL (FOR WOMEN) profile page.

The generic ingredient in MINOXIDIL (FOR WOMEN) is minoxidil. There are eight drug master file entries for this compound. Forty-five suppliers are listed for this compound. Additional details are available on the minoxidil profile page.
Summary for 074731
Formulation / Manufacturing:see details
Pharmacology for NDA: 074731
Physiological EffectArteriolar Vasodilation
Medical Subject Heading (MeSH) Categories for 074731
Suppliers and Packaging for NDA: 074731
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
MINOXIDIL (FOR MEN) minoxidil SOLUTION;TOPICAL 074731 ANDA Hi-Tech Pharmacal Co., Inc. 50383-001 50383-001-20 1 BOTTLE in 1 CARTON (50383-001-20) > 60 mL in 1 BOTTLE
MINOXIDIL (FOR MEN) minoxidil SOLUTION;TOPICAL 074731 ANDA Hi-Tech Pharmacal Co., Inc. 50383-001 50383-001-02 1 BOTTLE in 1 CARTON (50383-001-02) > 60 mL in 1 BOTTLE

Profile for product number 001

Active Rx/OTC/Discontinued:OTCDosage:SOLUTION;TOPICALStrength2%
Approval Date:Dec 24, 1996TE:RLD:No

Profile for product number 002

Active Rx/OTC/Discontinued:OTCDosage:SOLUTION;TOPICALStrength2%
Approval Date:May 11, 2005TE:RLD:No

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Serving leading biopharmaceutical companies globally:

Johnson and Johnson
Boehringer Ingelheim

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