DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1DR REDDYS
02 1MANKIND PHARMA
03 1ADAPTIS
04 1ALEMBIC
05 1APOTEX
06 1AUROBINDO PHARMA LTD
07 2BAYER HLTHCARE
08 1BAYER PHARMS
09 1CHARTWELL RX
10 1CROSSMEDIKA SA
11 1EPIC PHARMA LLC
12 1EUGIA PHARMA
13 1FRESENIUS KABI USA
14 1GLAND PHARMA LTD
15 2HARROW EYE
16 1HETERO LABS LTD V
17 2LUPIN LTD
18 1MSN
19 1MYLAN LABS LTD
20 1NATCO
21 1NORVIUM BIOSCIENCE
22 1SOMERSET THERAPS LLC
23 1SUNSHINE
24 1TEVA PHARMS
25 1TEVA PHARMS USA
26 1TORRENT
27 1UPSHER SMITH LABS
01 14SOLUTION/DROPS;OPHTHALMIC
02 1SOLUTION; OPHTHALMIC
03 3SOLUTION;INTRAVENOUS
04 11TABLET;ORAL
05 1Tablet; Oral
01 8DISCN
02 20RX
03 2Blank
01 2AVELOX
02 1AVELOX IN SODIUM CHLORIDE 0.8% IN PLASTIC CONTAINER
03 1MOXEZA
04 24MOXIFLOXACIN HYDROCHLORIDE
05 1MOXIFLOXACIN HYDROCHLORIDE IN SODIUM CHLORIDE 0.8% IN PLASTIC CONTAINER
06 1VIGAMOX
01 23No
02 5Yes
03 2Blank
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
RLD : No
TE Code : AB
Brand Name : MOXIFLOXACIN HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 400MG BASE
Approval Date : 2014-03-04
Application Number : 76938
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
Delivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.
RLD : No
TE Code : AT1
Brand Name : MOXIFLOXACIN HYDROCHLORIDE
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.5% BASE
Approval Date : 2025-01-27
Application Number : 217988
RX/OTC/DISCN : RX
RLD : No
TE Code : AT1
RLD : No
TE Code : AT1
Brand Name : MOXIFLOXACIN HYDROCHLORIDE
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.5% BASE
Approval Date : 2017-06-30
Application Number : 90080
RX/OTC/DISCN : RX
RLD : No
TE Code : AT1
RLD : Yes
TE Code :
Brand Name : AVELOX
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 400MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1999-12-10
Application Number : 21085
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : AVELOX IN SODIUM CHLORIDE 0.8% IN PLASTIC CONTAINER
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : 400MG/250ML (1.6MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 2001-11-30
Application Number : 21277
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD :
TE Code :
Brand Name : AVELOX
Dosage Form : Tablet; Oral
Dosage Strength : 400MG
Approval Date :
Application Number : 21334
RX/OTC/DISCN :
RLD :
TE Code :
RLD : Yes
TE Code : AT1
Brand Name : VIGAMOX
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.5% BASE
Approval Date : 2003-04-15
Application Number : 21598
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AT1
RLD : Yes
TE Code :
Brand Name : MOXEZA
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.5% BASE
Approval Date : 2010-11-19
Application Number : 22428
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code : AB
Brand Name : MOXIFLOXACIN HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 400MG BASE
Approval Date : 2014-02-18
Application Number : 77437
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD :
TE Code :
Brand Name : MOXIFLOXACIN HYDROCHLORIDE
Dosage Form : SOLUTION; OPHTHALMIC
Dosage Strength : 0.5%
Approval Date :
Application Number : 78073
RX/OTC/DISCN :
RLD :
TE Code :
