DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 4Dr. Reddy's Laboratories
02 3AAIPharma Services Corp.
03 2ANI Pharmaceuticals Inc
04 4Actavis Inc
05 4Ajanta Pharma Limited
06 4Alembic Pharmaceuticals Limited
07 4Amneal Pharmaceuticals
08 4Apotex Inc
09 4Aurobindo Pharma Limited
10 6Bayer AG
11 13Bristol Myers Squibb
12 4Chartwell Pharmaceuticals llc
13 1Fresenius Kabi USA
14 4Glenmark Pharmaceuticals
15 2H. Lundbeck AS
16 7Lannett Company, Inc.
17 4MSN Laboratories
18 4Novitium Pharma LLC
19 2PHARM ASSOC
20 3Pharmascience Inc.
21 4Prasco Laboratories
22 1Quad Pharma
23 4Rising Pharmaceuticals Inc
24 9Sandoz B2B
25 4TWi Pharmaceuticals
26 4Taro Pharmaceutical Industries
27 4Torrent Pharmaceuticals Limited
28 4Upsher-Smith Laboratories
29 4Zydus Lifesciences
01 4CONCENTRATE;ORAL
02 3ELIXIR;ORAL
03 1Fluphenazine 25Mg 1 Unit Parenteral Use
04 3INJ
05 3INJECTABLE;INJECTION
06 1Injectable; Injection
07 1SOLUTION FOR INJECTION
08 6TABLET
09 1TABLET, EXTENDED RELEASE;ORAL
10 96TABLET;ORAL
11 2Blank
01 32DISCN
02 3Originator
03 6Prescription
04 71RX
05 9Blank
01 1Dominans
02 3FLUPHENAZINE
03 1FLUPHENAZINE HCL
04 93FLUPHENAZINE HYDROCHLORIDE
05 3Modecate
06 1Moditen Depot
07 6PERMITIL
08 1PMS FLUPHENAZINE TAB 1MG
09 1PMS FLUPHENAZINE TAB 2MG
10 1PMS FLUPHENAZINE TAB 5MG
11 7PROLIXIN
12 1PROLIXIN ENANTHATE
13 1Siqualone decanoat
14 1Strong Dominans
01 6Canada
02 3Italy
03 3South Africa
04 1Sweden
05 108USA
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
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
Regulatory Info : DISCN
Registration Country : USA
Brand Name : FLUPHENAZINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Packaging :
Approval Date : 1987-12-18
Application Number : 88527
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : FLUPHENAZINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 2.5MG
Packaging :
Approval Date : 1987-12-18
Application Number : 88544
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : FLUPHENAZINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG
Packaging :
Approval Date : 1987-12-18
Application Number : 88550
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : FLUPHENAZINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 1MG
Packaging :
Approval Date : 1987-12-18
Application Number : 88555
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : FLUPHENAZINE HYDROCHLORIDE
Dosage Form : CONCENTRATE;ORAL
Dosage Strength : 5MG/ML
Packaging :
Approval Date : 1991-08-30
Application Number : 73058
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : FLUPHENAZINE HYDROCHLORIDE
Dosage Form : ELIXIR;ORAL
Dosage Strength : 2.5MG/5ML
Packaging :
Approval Date : 1993-04-29
Application Number : 81310
Regulatory Info : DISCN
Registration Country : USA
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
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
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
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
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
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
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
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
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
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
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
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
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PROLIXIN ENANTHATE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 25MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 16110
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PROLIXIN
Dosage Form : CONCENTRATE;ORAL
Dosage Strength : 5MG/ML
Packaging :
Approval Date : 1985-11-07
Application Number : 70533
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : FLUPHENAZINE HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 2.5MG/ML
Packaging :
Approval Date : 1987-04-16
Application Number : 89556
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : FLUPHENAZINE HYDROCHLORIDE
Dosage Form : ELIXIR;ORAL
Dosage Strength : 2.5MG/5ML
Packaging :
Approval Date : 1996-08-21
Application Number : 40146
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : FLUPHENAZINE HYDROCHLORIDE
Dosage Form : CONCENTRATE;ORAL
Dosage Strength : 5MG/ML
Packaging :
Approval Date : 1996-09-16
Application Number : 74725
Regulatory Info : RX
Registration Country : USA
Regulatory Info :
Registration Country : USA
Brand Name : FLUPHENAZINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Packaging :
Approval Date :
Application Number : 89585
Regulatory Info :
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : FLUPHENAZINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG
Packaging :
Approval Date : 1987-10-16
Application Number : 89586
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : FLUPHENAZINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 1MG
Packaging :
Approval Date : 1987-10-16
Application Number : 89586
Regulatory Info : DISCN
Registration Country : USA
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