Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
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 1FRESENIUS KABI USA
13 1GLAND PHARMA LTD
14 2HAINAN POLY
15 1HIKMA
16 2HOSPIRA
17 3LUPIN LTD
18 2NORVIUM BIOSCIENCE
19 2NOVEL LABS INC
20 1PF PRISM CV
21 8PFIZER
22 1PHARMOBEDIENT
23 5PLIVA
24 2RISING
25 5SANDOZ
26 1SANDOZ INC
27 1SLATE RUN PHARMA
28 1SUN PHARM INDS LTD
29 3SUNSHINE
30 1TARO
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
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Dosage Strength : EQ 250MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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
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
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