Synergice, a Strides Pharma initiative, is a new gen B2B platform for diverse portofolio needs.
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01 1STRIDES PHARMA
02 1AAIPHARMA LLC
03 1AUROBINDO PHARMA USA
04 1CHARTWELL RX
05 1COSETTE
06 1ENCUBE
07 1ESJAY PHARMA
08 1FOUGERA PHARMS
09 1HERITAGE PHARMA
10 1INA PHARMS
11 2JANSSEN PHARMA
12 2JANSSEN PHARMS
13 1KRAMER
14 1NORVIUM BIOSCIENCE
15 1NOVITIUM PHARMA
16 2PADAGIS ISRAEL
17 1SENORES PHARMS
18 1SUN PHARM INDUSTRIES
19 2TARO
20 2TEVA
21 1TRUPHARMA
22 1XIROMED
23 1ZYDUS LIFESCIENCES
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01 3AEROSOL, FOAM;TOPICAL
02 6CREAM;TOPICAL
03 1GEL;TOPICAL
04 6SHAMPOO;TOPICAL
05 1SUSPENSION;ORAL
06 11TABLET;ORAL
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01 12DISCN
02 1OTC
03 15RX
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01 1EXTINA
02 20KETOCONAZOLE
03 1KETOZOLE
04 4NIZORAL
05 1NIZORAL ANTI-DANDRUFF
06 1XOLEGEL
01 22No
02 6Yes
RLD : No
TE Code : AB
Brand Name : KETOCONAZOLE
Dosage Form : TABLET;ORAL
Dosage Strength : 200MG
Approval Date : 2018-06-18
Application Number : 210457
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code :
Brand Name : KETOCONAZOLE
Dosage Form : TABLET;ORAL
Dosage Strength : 200MG
Approval Date : 1999-06-15
Application Number : 74971
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
Brand Name : NIZORAL
Dosage Form : TABLET;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Dosage Strength : 200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 : 18533
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : NIZORAL
Dosage Form : CREAM;TOPICAL
Dosage Strength : 2% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1985-12-31
Application Number : 19084
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : NIZORAL
Dosage Form : SHAMPOO;TOPICAL
Dosage Strength : 2% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1990-08-31
Application Number : 19927
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
Brand Name : NIZORAL
Dosage Form : SUSPENSION;ORAL
Dosage Strength : 100MG/5ML
Approval Date : 1986-11-07
Application Number : 70767
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
Brand Name : NIZORAL ANTI-DANDRUFF
Dosage Form : SHAMPOO;TOPICAL
Dosage Strength : 1%
Approval Date : 1997-10-10
Application Number : 20310
RX/OTC/DISCN : OTC
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : EXTINA
Dosage Form : AEROSOL, FOAM;TOPICAL
Dosage Strength : 2% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 2007-06-12
Application Number : 21738
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
Brand Name : KETOCONAZOLE
Dosage Form : TABLET;ORAL
Dosage Strength : 200MG
Approval Date : 1999-06-15
Application Number : 75273
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
Brand Name : XOLEGEL
Dosage Form : GEL;TOPICAL
Dosage Strength : 2%
Approval Date : 2006-07-28
Application Number : 21946
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
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