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Approved Drug Products containing NCGC00024666-05 listed in the FDA Orange Book. Original Data : FDA Website

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01 2TARO

02 3APOTEX INC

03 2AUROBINDO PHARMA

04 2AUROBINDO PHARMA LTD

05 1AVACOR PRODS

06 1BAUSCH AND LOMB

07 1COPLEY PHARM

08 2ENDO OPERATIONS

09 2HIKMA

10 5JOHNSON AND JOHNSON

11 2L PERRIGO CO

12 4P AND L

13 1PERRIGO

14 1PERRIGO NEW YORK

15 1PERRIGO PHARMA INTL

16 2PFIZER

17 2PURE SOURCE

18 2QUANTUM PHARMICS

19 2ROYCE LABS

20 2SIGHT PHARMS

21 2SUN PHARM INDUSTRIES

22 1TEVA

23 1USL PHARMA

24 2WATSON LABS

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PharmaCompass

01

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MINOXIDIL

Brand Name : MINOXIDIL (FOR MEN)

Dosage Form : AEROSOL, FOAM;TOPICAL

Dosage Strength : 5%

Approval Date : 2018-12-31

Application Number : 209074

RX/OTC/DISCN : OTC

RLD : No

TE Code :

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02

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MINOXIDIL

Brand Name : MINOXIDIL (FOR WOMEN)

Dosage Form : AEROSOL, FOAM;TOPICAL

Dosage Strength : 5%

Approval Date : 2019-04-22

Application Number : 209074

RX/OTC/DISCN : OTC

RLD : No

TE Code :

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03

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MINOXIDIL

Brand Name : MINOXIDIL

Dosage Form : TABLET;ORAL

Dosage Strength : 2.5MG

Approval Date : 1987-03-03

Application Number : 71344

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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04

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MINOXIDIL

Brand Name : ROGAINE (FOR MEN)

Dosage Form : SOLUTION;TOPICAL

Dosage Strength : 2%

Approval Date : 1996-02-09

Application Number : 19501

RX/OTC/DISCN : OTC

RLD : Yes

TE Code :

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05

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MINOXIDIL

Brand Name : ROGAINE (FOR WOMEN)

Dosage Form : SOLUTION;TOPICAL

Dosage Strength : 2%

Approval Date : 1996-02-09

Application Number : 19501

RX/OTC/DISCN : OTC

RLD : Yes

TE Code :

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06

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MINOXIDIL

Brand Name : ROGAINE EXTRA STRENGTH (FOR MEN)

Dosage Form : SOLUTION;TOPICAL

Dosage Strength : 5%

Approval Date : 1997-11-14

Application Number : 20834

RX/OTC/DISCN : OTC

RLD : Yes

TE Code :

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07

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MINOXIDIL

Brand Name : MENS ROGAINE

Dosage Form : AEROSOL, FOAM;TOPICAL

Dosage Strength : 5%

Approval Date : 2006-01-20

Application Number : 21812

RX/OTC/DISCN : OTC

RLD : Yes

TE Code :

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08

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MINOXIDIL

Brand Name : WOMENS ROGAINE

Dosage Form : AEROSOL, FOAM;TOPICAL

Dosage Strength : 5%

Approval Date : 2014-02-28

Application Number : 21812

RX/OTC/DISCN : OTC

RLD : Yes

TE Code :

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09

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MINOXIDIL

Brand Name : LONITEN

Dosage Form : TABLET;ORAL

Dosage Strength : 2.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 18154

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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10

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MINOXIDIL

Brand Name : LONITEN

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 18154

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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