01 3APOTEX INC
02 2AUROBINDO PHARMA
03 2AUROBINDO PHARMA LTD
04 1AVACOR PRODS
05 1BAUSCH AND LOMB
06 1COPLEY PHARM
07 2ENDO OPERATIONS
08 2HIKMA
09 5JOHNSON AND JOHNSON
10 2L PERRIGO CO
11 4P AND L
12 1PERRIGO
13 1PERRIGO NEW YORK
14 1PERRIGO PHARMA INTL
15 2PFIZER
16 2PURE SOURCE
17 2QUANTUM PHARMICS
18 2ROYCE LABS
19 2SIGHT PHARMS
20 2SUN PHARM INDUSTRIES
21 2TARO
22 1TEVA
23 1USL PHARMA
24 2WATSON LABS
01 9AEROSOL, FOAM;TOPICAL
02 24SOLUTION;TOPICAL
03 13TABLET;ORAL
01 20DISCN
02 20OTC
03 6RX
01 2LONITEN
02 1MENS ROGAINE
03 2MINODYL
04 10MINOXIDIL
05 12MINOXIDIL (FOR MEN)
06 7MINOXIDIL (FOR WOMEN)
07 6MINOXIDIL EXTRA STRENGTH (FOR MEN)
08 1ROGAINE (FOR MEN)
09 1ROGAINE (FOR WOMEN)
10 1ROGAINE EXTRA STRENGTH (FOR MEN)
11 2THEROXIDIL
12 1WOMENS ROGAINE
01 39No
02 7Yes
RLD : No
TE Code : AB
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
RLD : No
TE Code : AB
Brand Name : MINOXIDIL
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG
Approval Date : 1987-03-03
Application Number : 71345
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : Yes
TE Code :
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 :
RLD : Yes
TE Code :
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 :
RLD : Yes
TE Code :
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 :
RLD : Yes
TE Code :
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 :
RLD : Yes
TE Code :
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 :
RLD : Yes
TE Code :
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Dosage Strength : 2.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 :
RLD : Yes
TE Code :
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 :
RLD : No
TE Code :
Brand Name : MINODYL
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG
Approval Date : 1987-03-19
Application Number : 71534
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
LOOKING FOR A SUPPLIER?
