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01 4Dr. Reddy's Laboratories

02 4Taro Pharmaceutical Industries

03 3AAIPharma Services Corp.

04 2ANI Pharmaceuticals Inc

05 4Actavis Inc

06 4Ajanta Pharma Limited

07 4Alembic Pharmaceuticals Limited

08 4Amneal Pharmaceuticals

09 4Apotex Inc

10 4Aurobindo Pharma Limited

11 6Bayer AG

12 13Bristol Myers Squibb

13 4Chartwell Pharmaceuticals llc

14 1Fresenius Kabi USA

15 4Glenmark Pharmaceuticals

16 2H. Lundbeck AS

17 7Lannett Company, Inc.

18 4MSN Laboratories

19 4Novitium Pharma LLC

20 2PHARM ASSOC

21 3Pharmascience Inc.

22 4Prasco Laboratories

23 1Quad Pharma

24 4Rising Pharmaceuticals Inc

25 9Sandoz B2B

26 4TWi Pharmaceuticals

27 4Torrent Pharmaceuticals Limited

28 4Upsher-Smith Laboratories

29 4Zydus Lifesciences

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PharmaCompass

01

  • 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

FLUPHENAZINE HYDROCHLORIDE

Brand Name : FLUPHENAZINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 1MG

Packaging :

Approval Date : 2021-01-07

Application Number : 214534

Regulatory Info : RX

Registration Country : USA

Dr Reddy 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

FLUPHENAZINE HYDROCHLORIDE

Brand Name : FLUPHENAZINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 2.5MG

Packaging :

Approval Date : 2021-01-07

Application Number : 214534

Regulatory Info : RX

Registration Country : USA

Dr Reddy 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

FLUPHENAZINE HYDROCHLORIDE

Brand Name : FLUPHENAZINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 5MG

Packaging :

Approval Date : 2021-01-07

Application Number : 214534

Regulatory Info : RX

Registration Country : USA

Dr Reddy Company Banner

04

  • 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

FLUPHENAZINE HYDROCHLORIDE

Brand Name : FLUPHENAZINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG

Packaging :

Approval Date : 2021-01-07

Application Number : 214534

Regulatory Info : RX

Registration Country : USA

Dr Reddy Company Banner

05

arrow
euroPLX 86 Munich
Not Confirmed

FLUPHENAZINE HYDROCHLORIDE

Brand Name : FLUPHENAZINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 1MG

Packaging :

Approval Date : 2022-04-14

Application Number : 215674

Regulatory Info : RX

Registration Country : USA

blank

06

arrow
euroPLX 86 Munich
Not Confirmed

FLUPHENAZINE HYDROCHLORIDE

Brand Name : FLUPHENAZINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 2.5MG

Packaging :

Approval Date : 2022-04-14

Application Number : 215674

Regulatory Info : RX

Registration Country : USA

blank

07

arrow
euroPLX 86 Munich
Not Confirmed

FLUPHENAZINE HYDROCHLORIDE

Brand Name : FLUPHENAZINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 5MG

Packaging :

Approval Date : 2022-04-14

Application Number : 215674

Regulatory Info : RX

Registration Country : USA

blank

08

arrow
euroPLX 86 Munich
Not Confirmed

FLUPHENAZINE HYDROCHLORIDE

Brand Name : FLUPHENAZINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG

Packaging :

Approval Date : 2022-04-14

Application Number : 215674

Regulatory Info : RX

Registration Country : USA

blank

09

euroPLX 86 Munich
Not Confirmed
arrow
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euroPLX 86 Munich
Not Confirmed

FLUPHENAZINE HYDROCHLORIDE

Brand Name : PERMITIL

Dosage Form : TABLET;ORAL

Dosage Strength : 0.25MG

Packaging :

Approval Date : 1982-01-01

Application Number : 12034

Regulatory Info : DISCN

Registration Country : USA

blank

10

euroPLX 86 Munich
Not Confirmed
arrow
arrow
euroPLX 86 Munich
Not Confirmed

FLUPHENAZINE HYDROCHLORIDE

Brand Name : PERMITIL

Dosage Form : TABLET;ORAL

Dosage Strength : 2.5MG

Packaging :

Approval Date : 1982-01-01

Application Number : 12034

Regulatory Info : DISCN

Registration Country : USA

blank

11

euroPLX 86 Munich
Not Confirmed
arrow
arrow
euroPLX 86 Munich
Not Confirmed

FLUPHENAZINE HYDROCHLORIDE

Brand Name : PERMITIL

Dosage Form : TABLET;ORAL

Dosage Strength : 5MG

Packaging :

Approval Date : 1982-01-01

Application Number : 12034

Regulatory Info : DISCN

Registration Country : USA

blank

12

euroPLX 86 Munich
Not Confirmed
arrow
arrow
euroPLX 86 Munich
Not Confirmed

FLUPHENAZINE HYDROCHLORIDE

Brand Name : PERMITIL

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG

Packaging :

Approval Date : 1982-01-01

Application Number : 12034

Regulatory Info : DISCN

Registration Country : USA

blank

13

euroPLX 86 Munich
Not Confirmed
arrow
arrow
euroPLX 86 Munich
Not Confirmed

FLUPHENAZINE HYDROCHLORIDE

Brand Name : PERMITIL

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : 1MG

Packaging :

Approval Date : 1982-01-01

Application Number : 12419

Regulatory Info : DISCN

Registration Country : USA

blank

14

euroPLX 86 Munich
Not Confirmed
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arrow
euroPLX 86 Munich
Not Confirmed

FLUPHENAZINE HYDROCHLORIDE

Brand Name : PERMITIL

Dosage Form : CONCENTRATE;ORAL

Dosage Strength : 5MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1982-01-01

Application Number : 16008

Regulatory Info : DISCN

Registration Country : USA

blank

15

euroPLX 86 Munich
Not Confirmed
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euroPLX 86 Munich
Not Confirmed

FLUPHENAZINE HYDROCHLORIDE

Brand Name : PROLIXIN

Dosage Form : TABLET;ORAL

Dosage Strength : 2.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1982-01-01

Application Number : 11751

Regulatory Info : DISCN

Registration Country : USA

blank

16

euroPLX 86 Munich
Not Confirmed
arrow
arrow
euroPLX 86 Munich
Not Confirmed

FLUPHENAZINE HYDROCHLORIDE

Brand Name : PROLIXIN

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1982-01-01

Application Number : 11751

Regulatory Info : DISCN

Registration Country : USA

blank

17

euroPLX 86 Munich
Not Confirmed
arrow
arrow
euroPLX 86 Munich
Not Confirmed

FLUPHENAZINE HYDROCHLORIDE

Brand Name : PROLIXIN

Dosage Form : TABLET;ORAL

Dosage Strength : 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1982-01-01

Application Number : 11751

Regulatory Info : DISCN

Registration Country : USA

blank

18

euroPLX 86 Munich
Not Confirmed
arrow
arrow
euroPLX 86 Munich
Not Confirmed

FLUPHENAZINE HYDROCHLORIDE

Brand Name : PROLIXIN

Dosage Form : TABLET;ORAL

Dosage Strength : 1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1982-01-01

Application Number : 11751

Regulatory Info : DISCN

Registration Country : USA

blank

19

euroPLX 86 Munich
Not Confirmed
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arrow
euroPLX 86 Munich
Not Confirmed

FLUPHENAZINE HYDROCHLORIDE

Brand Name : PROLIXIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 2.5MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1982-01-01

Application Number : 11751

Regulatory Info : DISCN

Registration Country : USA

blank

20

euroPLX 86 Munich
Not Confirmed
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arrow
euroPLX 86 Munich
Not Confirmed

FLUPHENAZINE HYDROCHLORIDE

Brand Name : PROLIXIN

Dosage Form : ELIXIR;ORAL

Dosage Strength : 2.5MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1982-01-01

Application Number : 12145

Regulatory Info : DISCN

Registration Country : USA

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