01 2Orion Corporation
02 4AAIPharma Services Corp.
03 4ANI Pharmaceuticals Inc
04 15Actavis Inc
05 4Appco Pharmaceutical Corp
06 19Bayer AG
07 5Chartwell Pharmaceuticals llc
08 4Fosun Pharmaceutical
09 5IVAX Pharmaceuticals Inc
10 4Jubilant Generics
11 1Laboratorios ERN
12 4Macleods Pharmaceuticals Limited
13 6Merck & Co
14 5New River Pharmaceuticals
15 3ORIFARM GROUP AS
16 4PH HEALTH
17 1PHARM ASSOC
18 5Par Pharmaceutical
19 5Pharmascience Inc.
20 4Rising Pharmaceuticals Inc
21 7Sandoz B2B
22 4Sun Pharmaceutical Industries Limited
23 13Viatris
24 4WILSHIRE PHARMS INC
25 4Zydus Pharmaceuticals
01 1Antic-calc Tablet, Film Coated
02 2CONCENTRATE;ORAL
03 3Film Coated Tablet
04 1INJECTABLE;INJECTION
05 4Injectable Solution
06 1Injection fluid, resolution
07 1LIQUID
08 1Oral Drops
09 1SYRUP;ORAL
10 8TABLET
11 1TABLET, EXTENDED RELEASE;ORAL
12 4TABLET; ORAL
13 99TABLET;ORAL
14 2Tablet
15 7Blank
01 1Approved
02 1Authorized
03 60DISCN
04 8Deregistered
05 9Prescription
06 41RX
07 16Blank
01 1Decentan
02 1ETRAFON 2-10
03 1ETRAFON 2-25
04 1ETRAFON-A
05 1ETRAFON-FORTE
06 4Mutabon
07 52PERPHENAZINE
08 43PERPHENAZINE AND AMITRIPTYLINE HYDROCHLORIDE
09 1PMS PERPHENAZINE CONCENTRATE LIQ 3.2MG/ML
10 1PMS PERPHENAZINE TAB 16MG
11 1PMS PERPHENAZINE TAB 2MG
12 1PMS PERPHENAZINE TAB 4MG
13 1PMS PERPHENAZINE TAB 8MG
14 1TRIAVIL 2-10
15 1TRIAVIL 2-25
16 1TRIAVIL 4-10
17 1TRIAVIL 4-25
18 1TRIAVIL 4-50
19 8TRILAFON
20 4Trilafon
21 3Trilafon Decanoate
22 1Trilafon Dekanoat
23 1Trilafon Enantat
24 1Trilafon Prolongatum
25 4Trilaphone
01 9Canada
02 7Italy
03 2Norway
04 1Spain
05 9Sweden
06 108USA
Regulatory Info :
Registration Country : Norway
Brand Name : Trilafon Dekanoat
Dosage Form : Injection fluid, resolution
Dosage Strength : 108,2 mg/ml
Packaging : Ampoule
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Trilafon Decanoate
Dosage Form : Injectable Solution
Dosage Strength : 108mg/ml
Packaging :
Approval Date : 18/09/1987
Application Number : 19870918000021
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : DISCN
Registration Country : USA
Brand Name : TRILAFON
Dosage Form : TABLET;ORAL
Dosage Strength : 2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 10775
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : TRILAFON
Dosage Form : TABLET;ORAL
Dosage Strength : 4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 10775
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : TRILAFON
Dosage Form : TABLET;ORAL
Dosage Strength : 8MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 10775
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : TRILAFON
Dosage Form : TABLET;ORAL
Dosage Strength : 16MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 10775
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : TRILAFON
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 5MG/ML
Packaging :
Approval Date : 1982-01-01
Application Number : 11213
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : TRILAFON
Dosage Form : SYRUP;ORAL
Dosage Strength : 2MG/5ML
Packaging :
Approval Date : 1982-01-01
Application Number : 11294
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : TRILAFON
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 8MG
Packaging :
Approval Date : 1982-01-01
Application Number : 11361
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : TRILAFON
Dosage Form : CONCENTRATE;ORAL
Dosage Strength : 16MG/5ML
Packaging :
Approval Date : 1982-01-01
Application Number : 11557
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
AMITRIPTYLINE HYDROCHLORIDE; PERPHENAZINE
Brand Name : ETRAFON-A
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG;4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 14713
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
AMITRIPTYLINE HYDROCHLORIDE; PERPHENAZINE
Brand Name : ETRAFON 2-25
Dosage Form : TABLET;ORAL
Dosage Strength : 25MG;2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 14713
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
AMITRIPTYLINE HYDROCHLORIDE; PERPHENAZINE
Brand Name : ETRAFON-FORTE
Dosage Form : TABLET;ORAL
Dosage Strength : 25MG;4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 14713
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
AMITRIPTYLINE HYDROCHLORIDE; PERPHENAZINE
Brand Name : ETRAFON 2-10
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG;2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 14713
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
AMITRIPTYLINE HYDROCHLORIDE; PERPHENAZINE
Brand Name : TRIAVIL 2-25
Dosage Form : TABLET;ORAL
Dosage Strength : 25MG;2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 14715
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
AMITRIPTYLINE HYDROCHLORIDE; PERPHENAZINE
Brand Name : TRIAVIL 4-10
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG;4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 14715
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
AMITRIPTYLINE HYDROCHLORIDE; PERPHENAZINE
Brand Name : TRIAVIL 2-10
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG;2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 14715
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
AMITRIPTYLINE HYDROCHLORIDE; PERPHENAZINE
Brand Name : TRIAVIL 4-25
Dosage Form : TABLET;ORAL
Dosage Strength : 25MG;4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 14715
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
AMITRIPTYLINE HYDROCHLORIDE; PERPHENAZINE
Brand Name : TRIAVIL 4-50
Dosage Form : TABLET;ORAL
Dosage Strength : 50MG;4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 14715
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : PERPHENAZINE
Dosage Form : TABLET;ORAL
Dosage Strength : 2MG
Packaging :
Approval Date : 1998-12-31
Application Number : 40226
Regulatory Info : RX
Registration Country : USA
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