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01 10 Oxycodone Hydrochloride; Naloxone Hydrochloride Anhydrous

02 1Ambroxol Hydrochloride

03 1Atropine Sulfate Monohydrate; Hydromorphone Hydrochloride

04 7Buprenorfin

05 7Buprenorphine

06 1Choline Salicylate

07 27Fluticasone Propionate; Formoterol Fumarate Dihydrate

08 6Fluticasone Propionate; Formoterol Fumarate Dihydric

09 3Flutikasonpropionat, Formoterolfumaratdihydrat

10 3Formoterol; Fluticasone

11 7Formoterol; Fluticasone Furoate

12 42Hydromorphone Hydrochloride

13 1Ibuprofen; Codeine Phosphate Hemihydrate

14 3Lidocaine Hydrochloride Monohydrate; Amylmetacresol; 2,4-Dichlorobenzyl Alcohol

15 1Lidocaine; Amylmetacresol; 2,4-Dichlorobenzylic Alcohol

16 2Malathion

17 12Morfinhemisulfat-2,5-Hydrat

18 14Morphine

19 11Morphine Sulfate

20 2Morphine Sulfate Pentahydrate

21 19Morphine hemisulphate 2,5-hydrate

22 4Morphine sulfate

23 1Naloxone

24 2Naloxone Hydrochloride Dihydrate

25 16Naloxone Hydrochloride Dihydrate; Oxycodone Hydrochloride

26 6Naloxone Hydrochloride; Oxycodone Hydrochloride

27 54Oxycodone

28 5Oxycodone (oxycodone) hydrochloride

29 4Oxycodone (oxycodone) hydrochloride/naloxone hydrochloride dihydrate

30 49Oxycodone Hydrochloride

31 4Oxycodone; Naloxone

32 3Pegfilgrastim

33 7Povidone-Iodine

34 18Prednisone

35 2Rezafungin Acetate

36 14Tramadol Hydrochloride

37 9Tramadol hydrochloride

38 3Tramadolhydroklorid

39 1Zinc Sulfate Heptahydrate; Zinc Oxide

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PharmaCompass

01

Brand Name : Targin mg

AAPS
Not Confirmed
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Brand Name : Targin mg

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AAPS
Not Confirmed

Mundipharma

Dosage Form : Modified Release Tablet

Dosage Strength : 10mg;5mg

Packaging :

Brand Name : Targin mg

Approval Date : 13/11/2009

Application Number : 58683

Regulatory Info : Allowed

Registration Country : Switzerland

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02

Brand Name : Targin mg

AAPS
Not Confirmed
arrow

Brand Name : Targin mg

arrow
AAPS
Not Confirmed

Mundipharma

Dosage Form : Modified Release Tablet

Dosage Strength : 20mg;10mg

Packaging :

Brand Name : Targin mg

Approval Date : 13/11/2009

Application Number : 58683

Regulatory Info : Allowed

Registration Country : Switzerland

blank

03

Brand Name : Targin

AAPS
Not Confirmed
arrow

Brand Name : Targin

arrow
AAPS
Not Confirmed

Mundipharma

Dosage Form : Modified Release Tablet

Dosage Strength : 5mg;2.5mg

Packaging :

Brand Name : Targin

Approval Date : 13/11/2009

Application Number : 58683

Regulatory Info : Allowed

Registration Country : Switzerland

blank

04

Brand Name : Targin mg

AAPS
Not Confirmed
arrow

Brand Name : Targin mg

arrow
AAPS
Not Confirmed

Mundipharma

Dosage Form : Modified Release Tablet

Dosage Strength : 40mg;20mg

Packaging :

Brand Name : Targin mg

Approval Date : 13/11/2009

Application Number : 58683

Regulatory Info : Allowed

Registration Country : Switzerland

blank

05

Brand Name : Targin mg

AAPS
Not Confirmed
arrow

Brand Name : Targin mg

arrow
AAPS
Not Confirmed

Mundipharma

Dosage Form : Modified Release Tablet

Dosage Strength : 60mg;30mg

Packaging :

Brand Name : Targin mg

Approval Date : 13/11/2009

Application Number : 58683

Regulatory Info : Allowed

Registration Country : Switzerland

blank

06

Brand Name : Targin mg

AAPS
Not Confirmed
arrow

Brand Name : Targin mg

arrow
AAPS
Not Confirmed

Mundipharma

Dosage Form : Modified Release Tablet

Dosage Strength : 80mg;40mg

Packaging :

Brand Name : Targin mg

Approval Date : 13/11/2009

Application Number : 58683

Regulatory Info : Allowed

Registration Country : Switzerland

blank

07

Brand Name : OxycodoneNaloxone Mu...

AAPS
Not Confirmed
arrow

Brand Name : OxycodoneNaloxone Mu...

arrow
AAPS
Not Confirmed

Mundipharma

Dosage Form : Modified Release Tablet

Dosage Strength : 10mg;5mg

Packaging :

Brand Name : OxycodoneNaloxone Mundipharma...

Approval Date : 17/05/2023

Application Number : 69358

Regulatory Info : Allowed

Registration Country : Switzerland

blank

08

Brand Name : OxycodoneNaloxone Mu...

AAPS
Not Confirmed
arrow

Brand Name : OxycodoneNaloxone Mu...

arrow
AAPS
Not Confirmed

Mundipharma

Dosage Form : Modified Release Tablet

Dosage Strength : 20mg;10mg

Packaging :

Brand Name : OxycodoneNaloxone Mundipharma...

Approval Date : 17/05/2023

Application Number : 69358

Regulatory Info : Allowed

Registration Country : Switzerland

blank

09

Brand Name : OxycodoneNaloxone Mu...

AAPS
Not Confirmed
arrow

Brand Name : OxycodoneNaloxone Mu...

arrow
AAPS
Not Confirmed

Mundipharma

Dosage Form : Modified Release Tablet

Dosage Strength : 5mg;2.5mg

Packaging :

Brand Name : OxycodoneNaloxone Mundipharma...

Approval Date : 17/05/2023

Application Number : 69358

Regulatory Info : Allowed

Registration Country : Switzerland

blank

10

Brand Name : OxycodoneNaloxone Mu...

AAPS
Not Confirmed
arrow

Brand Name : OxycodoneNaloxone Mu...

arrow
AAPS
Not Confirmed

Mundipharma

Dosage Form : Modified Release Tablet

Dosage Strength : 40mg;20mg

Packaging :

Brand Name : OxycodoneNaloxone Mundipharma...

Approval Date : 17/05/2023

Application Number : 69358

Regulatory Info : Allowed

Registration Country : Switzerland

blank
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Mundipharma is a supplier offers 1 products (APIs, Excipients or Intermediates).

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