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

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01 4Dr. Reddy's Laboratories
02 4Breckenridge Pharmaceutical
03 3AAIPharma Services Corp.
04 2ANI Pharmaceuticals Inc
05 4Actavis Inc
06 4Ajanta Pharma Limited
07 4Alembic Pharmaceuticals Limited
08 4Amneal Pharmaceuticals
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11 6Bayer AG
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14 1Fresenius Kabi USA
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16 2H. Lundbeck AS
17 4Hetero Drugs
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19 7Lannett Company, Inc.
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22 2PHARM ASSOC
23 3Pharmascience Inc.
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25 1Quad Pharma
26 4Rising Pharmaceuticals Inc
27 5Sandoz B2B
28 4TWi Pharmaceuticals
29 4Taro Pharmaceutical Industries
30 4Torrent Pharmaceuticals Limited
31 4Upsher-Smith Laboratories
32 4Zydus Lifesciences
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01 4CONCENTRATE;ORAL
02 3ELIXIR;ORAL
03 1Fluphenazine 25Mg 1 Unit Parenteral Use
04 3INJ
05 3INJECTABLE;INJECTION
06 1Injectable Solution
07 1Injectable; Injection
08 6TABLET
09 1TABLET, EXTENDED RELEASE;ORAL
10 100TABLET;ORAL
11 1Tablet
12 2Blank
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01 36DISCN
02 1Deregistered
03 3Originator
04 6Prescription
05 71RX
06 9Blank
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01 1Dominans
02 3FLUPHENAZINE
03 1FLUPHENAZINE HCL
04 97FLUPHENAZINE HYDROCHLORIDE
05 3Modecate
06 1Moditen Depot
07 1Moditen® depo
08 6PERMITIL
09 1PMS FLUPHENAZINE TAB 1MG
10 1PMS FLUPHENAZINE TAB 2MG
11 1PMS FLUPHENAZINE TAB 5MG
12 7PROLIXIN
13 1PROLIXIN ENANTHATE
14 1Siqualone
15 1Strong Dominans
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01 6Canada
02 3Italy
03 1Moldova
04 3South Africa
05 1Sweden
06 112USA
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : RX
Registration Country : USA
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
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Regulatory Info : RX
Registration Country : USA
Brand Name : FLUPHENAZINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 1MG
Packaging :
Approval Date : 2022-11-15
Application Number : 216891
Regulatory Info : RX
Registration Country : USA
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : RX
Registration Country : USA
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
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : RX
Registration Country : USA
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
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : RX
Registration Country : USA
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
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Regulatory Info : RX
Registration Country : USA
Brand Name : FLUPHENAZINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 2.5MG
Packaging :
Approval Date : 2022-11-15
Application Number : 216891
Regulatory Info : RX
Registration Country : USA
Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass.
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Regulatory Info : RX
Registration Country : USA
Brand Name : FLUPHENAZINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Packaging :
Approval Date : 2022-11-15
Application Number : 216891
Regulatory Info : RX
Registration Country : USA
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Regulatory Info : RX
Registration Country : USA
Brand Name : FLUPHENAZINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG
Packaging :
Approval Date : 2022-11-15
Application Number : 216891
Regulatory Info : RX
Registration Country : USA
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Regulatory Info : DISCN
Registration Country : USA
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

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Regulatory Info : DISCN
Registration Country : USA
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

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Regulatory Info : DISCN
Registration Country : USA
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

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Regulatory Info : DISCN
Registration Country : USA
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

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Regulatory Info : DISCN
Registration Country : USA
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

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Regulatory Info : DISCN
Registration Country : USA
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

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Regulatory Info : DISCN
Registration Country : USA
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

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Regulatory Info : DISCN
Registration Country : USA
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

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Regulatory Info : DISCN
Registration Country : USA
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

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Regulatory Info : DISCN
Registration Country : USA
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

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Regulatory Info : DISCN
Registration Country : USA
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

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Regulatory Info : DISCN
Registration Country : USA
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
