Synergice, a Strides Pharma initiative, is a new gen B2B platform for diverse portofolio needs.
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01 2STRIDES PHARMA
02 3ALEMBIC
03 2AMNEAL
04 3APOTEX CORP
05 4AUROBINDO PHARMA LTD
06 1AUROBINDO PHARMA USA
07 3BIONPHARMA
08 5CHARTWELL RX
09 3CSPC OUYI
10 2EPIC PHARMA LLC
11 1EUGIA PHARMA
12 1EXTROVIS
13 1FRESENIUS KABI USA
14 1GLAND PHARMA LTD
15 1HIKMA
16 2HOSPIRA
17 3LUPIN LTD
18 2NOVEL LABS INC
19 1PF PRISM CV
20 8PFIZER
21 3PHARMOBEDIENT
22 5PLIVA
23 1RISING
24 5SANDOZ
25 1SANDOZ INC
26 1SLATE RUN PHARMA
27 1SUN PHARM INDS LTD
28 3SUNSHINE
29 1TARO
30 3TEVA
31 2TEVA PARENTERAL
32 2TEVA PHARMS
33 1THEA PHARMA
34 2YUNG SHIN PHARM
35 2ZHEJIANG POLY PHARM
36 2ZYDUS LIFESCIENCES
37 2ZYDUS PHARMS
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01 1CAPSULE;ORAL
02 1FOR SUSPENSION, EXTENDED RELEASE;ORAL
03 24FOR SUSPENSION;ORAL
04 13INJECTABLE;INJECTION
05 1SOLUTION/DROPS;OPHTHALMIC
06 1SOLUTION; OPHTHALMIC
07 45TABLET;ORAL
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01 28DISCN
02 55RX
03 3Blank
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01 1AZASITE
02 76AZITHROMYCIN
03 8ZITHROMAX
04 1ZMAX
01 73No
02 10Yes
03 3Blank
RLD : No
TE Code : AB
Brand Name : AZITHROMYCIN
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 250MG BASE
Approval Date : 2022-07-15
Application Number : 215772
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : AZITHROMYCIN
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 500MG BASE
Approval Date : 2022-07-12
Application Number : 215773
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : Yes
TE Code :
Brand Name : ZITHROMAX
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 250MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1991-11-01
Application Number : 50670
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : ZITHROMAX
Dosage Form : FOR SUSPENSION;ORAL
Dosage Strength : EQ 1GM BASE/PACKET
Approval Date : 1994-09-28
Application Number : 50693
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code : AB
Brand Name : ZITHROMAX
Dosage Form : FOR SUSPENSION;ORAL
Dosage Strength : EQ 100MG BASE/5ML
Approval Date : 1995-10-19
Application Number : 50710
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Brand Name : ZITHROMAX
Dosage Form : FOR SUSPENSION;ORAL
Dosage Strength : EQ 200MG BASE/5ML
Approval Date : 1995-10-19
Application Number : 50710
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Brand Name : ZITHROMAX
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 250MG BASE
Approval Date : 1996-07-18
Application Number : 50711
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code :
Brand Name : ZITHROMAX
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 600MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1996-06-12
Application Number : 50730
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code : AP
Brand Name : ZITHROMAX
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 500MG BASE/VIAL
Approval Date : 1997-01-30
Application Number : 50733
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AP
RLD : Yes
TE Code : AB
Brand Name : ZITHROMAX
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 500MG BASE
Approval Date : 2002-05-24
Application Number : 50784
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB