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01 2Orion Corporation

02 1Dr. Reddy's Laboratories

03 1ADAPTIS

04 1ANGITA PHARMA INC.

05 1Alcon Inc

06 1Alembic Pharmaceuticals Limited

07 3Apotex Inc

08 1Auro Pharma Inc

09 2Aurobindo Pharma Limited

10 9Bayer AG

11 2Bio Labs

12 1CROSSMEDIKA SA

13 1Chartwell Pharmaceuticals llc

14 1Chongqing Huapont Pharmaceutical

15 1Epic Pharma. LLC.

16 2Focelite

17 1Fresenius Kabi AB Brunna

18 1Fresenius Kabi Austria

19 1Fresenius Kabi USA

20 1GLAND PHARMA LIMITED

21 2Greenco Biologicals

22 2Ha Noi CPC1 Pharmaceutical JSC

23 1Hanlim Pharmaceuticals Inc

24 2Harrow

25 1Hetero Drugs

26 2JAMP PHARMA

27 1KRKA Sverige AB

28 2Lupin Ltd

29 1MANTRA PHARMA INC

30 1MSN Laboratories

31 3Mepha Pharma

32 1Nabros Pharma

33 1Natco Pharma

34 1Nobel Ilac Sanayii Ve Ticaret A.S.

35 2Novartis Pharmaceuticals Corporation

36 4ORIFARM GROUP AS

37 1PRO DOC LIMITEE

38 1Paranova Läkemedel AB

39 1Pharmachim AB

40 1Pharmascience Inc.

41 1Polifarma

42 2RANBAXY LABORATORIES LIMITED

43 1Remedy Pharma

44 2SANIS HEALTH INC

45 5Sandoz B2B

46 3Spirig Healthcare

47 1Sunshine Lake Pharma

48 3Teva Pharmaceutical Industries

49 1Theon Pharmaceuticals

50 1Torrent Pharmaceuticals Limited

51 1Umedica Laboratories

52 1Upsher-Smith Laboratories

53 2Viatris

54 1Yangtze River Pharmaceutical Group

55 1Blank

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PharmaCompass

01

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Pharmtech & Ingredients
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

02

  • 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

03

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Pharmtech & Ingredients
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

04

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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MOXIFLOXACIN HYDROCHLORIDE

Brand Name : MOXIFLOXACIN HYDROCHLORIDE

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : EQ 0.5% BASE

Packaging :

Approval Date : 2019-02-13

Application Number : 209469

Regulatory Info : RX

Registration Country : USA

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05

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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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06

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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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07

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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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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08

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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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09

Pharmtech & Ingredients
Not Confirmed
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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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10

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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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11

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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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12

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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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13

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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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14

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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 : 208778

Regulatory Info : RX

Registration Country : USA

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15

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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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16

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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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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17

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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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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18

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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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19

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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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20

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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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21

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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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22

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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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23

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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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24

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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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25

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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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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26

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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MOXIFLOXACIN HYDROCHLORIDE

Brand Name : MOXIFLOXACIN HYDROCHLORIDE

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : EQ 0.5% BASE

Packaging :

Approval Date : 2021-02-10

Application Number : 212616

Regulatory Info : RX

Registration Country : USA

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27

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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 : RX

Registration Country : USA

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29

ADAPTIS

Country
Pharmtech & Ingredients
Not Confirmed
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ADAPTIS

Country
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Pharmtech & Ingredients
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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CROSSMEDIKA SA

Country
Pharmtech & Ingredients
Not Confirmed
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CROSSMEDIKA SA

Country
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Pharmtech & Ingredients
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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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