Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
01 1TARO
02 2STRIDES PHARMA
03 3ALEMBIC
04 2AMNEAL
05 3APOTEX CORP
06 4AUROBINDO PHARMA LTD
07 1AUROBINDO PHARMA USA
08 3BIONPHARMA
09 5CHARTWELL RX
10 3CSPC OUYI
11 2EPIC PHARMA LLC
12 1EUGIA PHARMA
13 1FRESENIUS KABI USA
14 1GLAND PHARMA LTD
15 2HAINAN POLY
16 1HIKMA
17 2HOSPIRA
18 3LUPIN LTD
19 2NORVIUM BIOSCIENCE
20 2NOVEL LABS INC
21 1PF PRISM CV
22 8PFIZER
23 1PHARMOBEDIENT
24 5PLIVA
25 2RISING
26 5SANDOZ
27 1SANDOZ INC
28 1SLATE RUN PHARMA
29 1SUN PHARM INDS LTD
30 3SUNSHINE
31 3TEVA
32 2TEVA PARENTERAL
33 2TEVA PHARMS
34 1THEA PHARMA
35 2YUNG SHIN PHARM
36 2ZYDUS LIFESCIENCES
37 2ZYDUS PHARMS
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
01 28DISCN
02 55RX
03 3Blank
01 1AZASITE
02 76AZITHROMYCIN
03 8ZITHROMAX
04 1ZMAX
01 73No
02 10Yes
03 3Blank
Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
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 :
Brand Name : AZITHROMYCIN
Dosage Form : FOR SUSPENSION;ORAL
Dosage Strength : EQ 200MG BASE/5ML
Approval Date : 2019-12-11
Application Number : 211521
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
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Dosage Strength : EQ 250MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 : RX
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
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