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01 2Aspen Pharmacare Holdings

02 2Orion Corporation

03 1Dr. Reddy's Laboratories

04 1Mankind Pharma

05 1ADAPTIS

06 1ANGITA PHARMA INC.

07 1Alcon Inc

08 1Alembic Pharmaceuticals Limited

09 3Apotex Inc

10 1Auro Pharma Inc

11 2Aurobindo Pharma Limited

12 4Austell Laboratories

13 14Bayer AG

14 2Bio Labs

15 1Bosch Pharmaceuticals

16 1CROSSMEDIKA SA

17 1Chartwell Pharmaceuticals llc

18 1Chongqing Huapont Pharmaceutical

19 1Cipla Medpro South Africa

20 2Dr Reddy's Laboratories (Pty) Ltd

21 1Epic Pharma. LLC.

22 2Focelite

23 1Fresenius Kabi AB Brunna

24 1Fresenius Kabi Austria

25 1Fresenius Kabi USA

26 1Fresenius SE & Co. KGaA

27 1GLAND PHARMA LIMITED

28 1Gen-Eye

29 2Greenco Biologicals

30 2Ha Noi CPC1 Pharmaceutical JSC

31 1Hanlim Pharmaceuticals Inc

32 2Harrow

33 2Hetero Drugs

34 2JAMP PHARMA

35 1KRKA Sverige AB

36 2Lupin Ltd

37 1MANTRA PHARMA INC

38 1MSN Laboratories

39 2Macleods Pharmaceuticals Limited

40 3Mepha Pharma

41 1NORVIUM BIOSCIENCE

42 1Nabros Pharma

43 1Natco Pharma

44 1Nobel Ilac Sanayii Ve Ticaret A.S.

45 2Novartis Pharmaceuticals Corporation

46 1Novartis South Africa (Pty) Ltd

47 4ORIFARM GROUP AS

48 1PRO DOC LIMITEE

49 1Paranova Läkemedel AB

50 1Pharma Dynamics

51 1Pharmachim AB

52 1Pharmascience Inc.

53 1Polifarma

54 1Remedy Pharma

55 2SANIS HEALTH INC

56 5Sandoz B2B

57 1Somerset Pharmaceuticals Inc

58 3Spirig Healthcare

59 6Sun Pharmaceutical Industries Limited

60 1Sunshine Lake Pharma

61 3Teva Pharmaceutical Industries

62 1Theon Pharmaceuticals

63 1Torrent Pharmaceuticals Limited

64 1Umedica Laboratories

65 1Upsher-Smith Laboratories

66 1Viatris

67 1Yangtze River Pharmaceutical Group

68 1Blank

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PharmaCompass

01

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Interphex
Not Confirmed

Moxifloxacin

Brand Name : Litares

Dosage Form : TAB

Dosage Strength : 400mg

Packaging : 5X1mg

Approval Date :

Application Number :

Regulatory Info : Generic

Registration Country : South Africa

Aspen API Comapny Banner

02

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Plastics Recycling EU
Not Confirmed

moxifloxacinhydroklorid

Brand Name : Moxifloxacin Orion

Dosage Form : FILMDRAGERAD TABLETT

Dosage Strength : 400 MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Sweden

Fermion Orion Company Banner

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

Regulatory Info : RX

Registration Country : USA

MOXIFLOXACIN HYDROCHLORIDE

Brand Name : MOXIFLOXACIN HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 400MG BASE

Packaging :

Approval Date : 2014-03-04

Application Number : 76938

Regulatory Info : RX

Registration Country : USA

Dr Reddy Company Banner

04

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDelivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.

Regulatory Info : RX

Registration Country : USA

MOXIFLOXACIN HYDROCHLORIDE

Brand Name : MOXIFLOXACIN HYDROCHLORIDE

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : EQ 0.5% BASE

Packaging :

Approval Date : 2025-01-27

Application Number : 217988

Regulatory Info : RX

Registration Country : USA

Company Banner

05

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Interphex
Not Confirmed

Moxifloxacin

Brand Name : Litares

Dosage Form : TAB

Dosage Strength : 400mg

Packaging : 10X1mg

Approval Date :

Application Number :

Regulatory Info : Generic

Registration Country : South Africa

Aspen API Comapny Banner

06

arrow
Interphex
Not Confirmed

moxifloxacinhydroklorid

Brand Name : Moxifloxacin Orion

Dosage Form : INFUSIONSVÄTSKA, LÖSNING

Dosage Strength : 400 MG/250 ML

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Sweden

Fermion Orion Company Banner

07

Interphex
Not Confirmed
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Interphex
Not Confirmed

MOXIFLOXACIN HYDROCHLORIDE

Brand Name : MOXIFLOXACIN HYDROCHLORIDE

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : EQ 0.5% BASE

Packaging :

Approval Date : 2017-06-30

Application Number : 90080

Regulatory Info : RX

Registration Country : USA

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08

Plastics Recycling EU
Not Confirmed
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Plastics Recycling EU
Not Confirmed

MOXIFLOXACIN HYDROCHLORIDE

Brand Name : MOXIFLOXACIN HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 400MG BASE

Packaging :

Approval Date : 2014-03-04

Application Number : 202632

Regulatory Info : RX

Registration Country : USA

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09

Plastics Recycling EU
Not Confirmed
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Plastics Recycling EU
Not Confirmed

MOXIFLOXACIN HYDROCHLORIDE

Brand Name : MOXIFLOXACIN HYDROCHLORIDE

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : EQ 0.5% BASE

Packaging :

Approval Date : 2017-10-04

Application Number : 206242

Regulatory Info : RX

Registration Country : USA

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10

Interphex
Not Confirmed
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Interphex
Not Confirmed

MOXIFLOXACIN HYDROCHLORIDE

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**

Packaging :

Approval Date : 1999-12-10

Application Number : 21085

Regulatory Info : DISCN

Registration Country : USA

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11

Interphex
Not Confirmed
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Interphex
Not Confirmed

MOXIFLOXACIN HYDROCHLORIDE

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**

Packaging :

Approval Date : 2001-11-30

Application Number : 21277

Regulatory Info : DISCN

Registration Country : USA

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12

Interphex
Not Confirmed
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Interphex
Not Confirmed

MOXIFLOXACIN HYDROCHLORIDE

Brand Name : AVELOX

Dosage Form : Tablet; Oral

Dosage Strength : 400MG

Packaging :

Approval Date :

Application Number : 21334

Regulatory Info :

Registration Country : USA

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13

Interphex
Not Confirmed
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Interphex
Not Confirmed

MOXIFLOXACIN HYDROCHLORIDE

Brand Name : MOXIFLOXACIN HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 400MG BASE

Packaging :

Approval Date : 2017-02-13

Application Number : 207285

Regulatory Info : RX

Registration Country : USA

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14

Interphex
Not Confirmed
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Interphex
Not Confirmed

MOXIFLOXACIN HYDROCHLORIDE

Brand Name : MOXIFLOXACIN HYDROCHLORIDE

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : EQ 0.5% BASE

Packaging :

Approval Date : 2017-11-09

Application Number : 202916

Regulatory Info : DISCN

Registration Country : USA

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15

Interphex
Not Confirmed
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Interphex
Not Confirmed

MOXIFLOXACIN HYDROCHLORIDE

Brand Name : MOXIFLOXACIN HYDROCHLORIDE

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : EQ 400MG BASE/250ML (EQ 1.6MG BASE/ML)

Packaging :

Approval Date : 2015-04-03

Application Number : 205572

Regulatory Info : RX

Registration Country : USA

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16

Interphex
Not Confirmed
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Interphex
Not Confirmed

MOXIFLOXACIN HYDROCHLORIDE

Brand Name : VIGAMOX

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : EQ 0.5% BASE

Packaging :

Approval Date : 2003-04-15

Application Number : 21598

Regulatory Info : RX

Registration Country : USA

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17

Interphex
Not Confirmed
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Interphex
Not Confirmed

MOXIFLOXACIN HYDROCHLORIDE

Brand Name : MOXEZA

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : EQ 0.5% BASE

Packaging :

Approval Date : 2010-11-19

Application Number : 22428

Regulatory Info : DISCN

Registration Country : USA

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18

Interphex
Not Confirmed
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Interphex
Not Confirmed

MOXIFLOXACIN HYDROCHLORIDE

Brand Name : MOXIFLOXACIN HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 400MG BASE

Packaging :

Approval Date : 2023-03-02

Application Number : 204836

Regulatory Info : RX

Registration Country : USA

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19

Plastics Recycling EU
Not Confirmed
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Plastics Recycling EU
Not Confirmed

MOXIFLOXACIN HYDROCHLORIDE

Brand Name : MOXIFLOXACIN HYDROCHLORIDE

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : EQ 0.5% BASE

Packaging :

Approval Date : 2014-09-04

Application Number : 202867

Regulatory Info : RX

Registration Country : USA

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20

Plastics Recycling EU
Not Confirmed
arrow
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Plastics Recycling EU
Not Confirmed

MOXIFLOXACIN HYDROCHLORIDE

Brand Name : MOXIFLOXACIN HYDROCHLORIDE

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : EQ 0.5% BASE

Packaging :

Approval Date : 2015-05-28

Application Number : 204079

Regulatory Info : RX

Registration Country : USA

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21

Plastics Recycling EU
Not Confirmed
arrow
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Plastics Recycling EU
Not Confirmed

MOXIFLOXACIN HYDROCHLORIDE

Brand Name : MOXIFLOXACIN HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 400MG BASE

Packaging :

Approval Date : 2017-09-22

Application Number : 208682

Regulatory Info : RX

Registration Country : USA

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22

Plastics Recycling EU
Not Confirmed
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Plastics Recycling EU
Not Confirmed

MOXIFLOXACIN HYDROCHLORIDE

Brand Name : MOXIFLOXACIN HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 400MG BASE

Packaging :

Approval Date : 2015-08-31

Application Number : 204635

Regulatory Info : DISCN

Registration Country : USA

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23

Interphex
Not Confirmed
arrow
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Interphex
Not Confirmed

MOXIFLOXACIN HYDROCHLORIDE

Brand Name : MOXIFLOXACIN HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 400MG BASE

Packaging :

Approval Date : 2018-09-28

Application Number : 206295

Regulatory Info : DISCN

Registration Country : USA

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24

Interphex
Not Confirmed
arrow
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Interphex
Not Confirmed

MOXIFLOXACIN HYDROCHLORIDE

Brand Name : MOXIFLOXACIN HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 400MG BASE

Packaging :

Approval Date : 2014-02-18

Application Number : 77437

Regulatory Info : RX

Registration Country : USA

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25

Interphex
Not Confirmed
arrow
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Interphex
Not Confirmed

MOXIFLOXACIN HYDROCHLORIDE

Brand Name : MOXIFLOXACIN HYDROCHLORIDE

Dosage Form : SOLUTION; OPHTHALMIC

Dosage Strength : 0.5%

Packaging :

Approval Date :

Application Number : 78073

Regulatory Info :

Registration Country : USA

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26

Interphex
Not Confirmed
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Interphex
Not Confirmed

MOXIFLOXACIN HYDROCHLORIDE

Brand Name : MOXIFLOXACIN HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 400MG BASE

Packaging :

Approval Date : 2014-04-03

Application Number : 200160

Regulatory Info : DISCN

Registration Country : USA

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27

Interphex
Not Confirmed
arrow
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Interphex
Not Confirmed

MOXIFLOXACIN HYDROCHLORIDE

Brand Name : MOXIFLOXACIN HYDROCHLORIDE IN SODIUM CHLORIDE 0.8% IN PLASTIC CONTAINER

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : 400MG/250ML (1.6MG/ML)

Packaging :

Approval Date : 2017-05-05

Application Number : 205833

Regulatory Info : RX

Registration Country : USA

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28

ADAPTIS

Country
Interphex
Not Confirmed
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ADAPTIS

Country
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Interphex
Not Confirmed

MOXIFLOXACIN HYDROCHLORIDE

Brand Name : MOXIFLOXACIN HYDROCHLORIDE

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : EQ 0.5% BASE

Packaging :

Approval Date : 2015-03-06

Application Number : 202525

Regulatory Info : RX

Registration Country : USA

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29

CROSSMEDIKA SA

Country
Interphex
Not Confirmed
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CROSSMEDIKA SA

Country
arrow
Interphex
Not Confirmed

MOXIFLOXACIN HYDROCHLORIDE

Brand Name : MOXIFLOXACIN HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 400MG BASE

Packaging :

Approval Date : 2016-01-14

Application Number : 205348

Regulatory Info : RX

Registration Country : USA

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30

NORVIUM BIOSCIENCE

Country
Interphex
Not Confirmed
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NORVIUM BIOSCIENCE

Country
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Interphex
Not Confirmed

MOXIFLOXACIN HYDROCHLORIDE

Brand Name : MOXIFLOXACIN HYDROCHLORIDE

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : EQ 0.5% BASE

Packaging :

Approval Date : 2020-03-30

Application Number : 206447

Regulatory Info : DISCN

Registration Country : USA

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