Rusan Pharma: Over 30 years of specializing in the treatment of Addiction and Pain Management.
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01 1CONCENTRATE;ORAL
02 1Capsule
03 3DC Granules
04 6DC Granules and Tablets
05 5FILM COATED PILL
06 6Film Coated Tablet
07 2INJECTABLE;INJECTION
08 1Injection
09 3Oral Solution
10 2SR Tablet
11 2TAB
12 31TABLET
13 10TABLET; ORAL
14 275TABLET;ORAL
15 14Tablet
16 7Tablet, film-coated
17 4Blank
01 205DISCN
02 3DMF Available|FDF Compliance-USP
03 7Generic
04 3Prescription
05 69RX
06 86Blank
01 1A-TRIP-10
02 1A-TRIP-25
03 5AMITID
04 6AMITRIL
05 1AMITRIPTYLINE
06 196AMITRIPTYLINE HYDROCHLORIDE
07 1AMITRIPTYLINE-10
08 1AMITRIPTYLINE-25
09 1AMITRIPTYLINE-50
10 2AMITRYN
11 4APO-AMITRIPTYLINE
12 6Amitriptyline Abcur
13 1Amitriptyline HCL
14 2Amitriptyline HCl 25 Kiara
15 2Amitriptyline Orifarm
16 13CHLORDIAZEPOXIDE AND AMITRIPTYLINE HYDROCHLORIDE
17 1DEPRELIO
18 1Diapatol
19 11ELAVIL
20 7ENDEP
21 1ETRAFON 2-10
22 1ETRAFON 2-25
23 1ETRAFON-A
24 1ETRAFON-FORTE
25 4JAMP-AMITRIPTYLINE
26 1LIMBITROL
27 1LIMBITROL DS
28 2Limbitryl
29 4MAR-AMITRIPTYLINE
30 43PERPHENAZINE AND AMITRIPTYLINE HYDROCHLORIDE
31 4PMS-AMITRIPTYLINE
32 1PMS-AMITRIPTYLINE TABLETS 10MG
33 1PMS-AMITRIPTYLINE TABLETS 25MG
34 1PMS-AMITRIPTYLINE TABLETS 50MG
35 1RELIDEP -10
36 1RELIDEP -25
37 1RELIDEP -50
38 1RELIDEP -75
39 1RELIDEP PLUS TAB
40 1RELIDEP PLUS-H
41 2Saroten
42 2Sarotex
43 1Sedans
44 1TRIAVIL 2-10
45 1TRIAVIL 2-25
46 1TRIAVIL 4-10
47 1TRIAVIL 4-25
48 1TRIAVIL 4-50
49 28Blank
01 26Canada
02 40India
03 4Italy
04 7Norway
05 2South Africa
06 1Spain
07 5Sweden
08 288USA
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Tablet
Dosage Strength : 10mg
Packaging : Pack Size 10x10
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info : RX
Registration Country : USA
Brand Name : AMITRIPTYLINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG
Packaging :
Approval Date : 2022-06-06
Application Number : 216243
Regulatory Info : RX
Registration Country : USA
Octavius has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
Regulatory Info : DMF Available|FDF Compliance-USP
Registration Country : India
Brand Name :
Dosage Form : DC Granules
Dosage Strength : 25MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : DMF Available|FDF Compliance-USP
Registration Country : India
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Tablet
Dosage Strength : 25mg
Packaging : Pack Size 10x10
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Injection
Dosage Strength : 10mg/ml
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info : RX
Registration Country : USA
Brand Name : AMITRIPTYLINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 25MG
Packaging :
Approval Date : 2022-06-06
Application Number : 216243
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : AMITRIPTYLINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 50MG
Packaging :
Approval Date : 2022-06-06
Application Number : 216243
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : AMITRIPTYLINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 75MG
Packaging :
Approval Date : 2022-06-06
Application Number : 216243
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : AMITRIPTYLINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 100MG
Packaging :
Approval Date : 2022-06-06
Application Number : 216243
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : AMITRIPTYLINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 150MG
Packaging :
Approval Date : 2022-06-06
Application Number : 216243
Regulatory Info : RX
Registration Country : USA
Octavius has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
Regulatory Info : DMF Available|FDF Compliance-USP
Registration Country : India
Brand Name :
Dosage Form : DC Granules
Dosage Strength : 50MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : DMF Available|FDF Compliance-USP
Registration Country : India
Octavius has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
Regulatory Info : DMF Available|FDF Compliance-USP
Registration Country : India
Brand Name :
Dosage Form : DC Granules
Dosage Strength : 100MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : DMF Available|FDF Compliance-USP
Registration Country : India
Regulatory Info : RX
Registration Country : USA
Brand Name : AMITRIPTYLINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 75MG
Packaging :
Approval Date : 2021-09-29
Application Number : 212654
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : AMITRIPTYLINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 100MG
Packaging :
Approval Date : 2021-09-29
Application Number : 212654
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : AMITRIPTYLINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 150MG
Packaging :
Approval Date : 2021-09-29
Application Number : 212654
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ELAVIL
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 : 12703
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ELAVIL
Dosage Form : TABLET;ORAL
Dosage Strength : 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 12703
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ELAVIL
Dosage Form : TABLET;ORAL
Dosage Strength : 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 12703
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ELAVIL
Dosage Form : TABLET;ORAL
Dosage Strength : 75MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 12703
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ELAVIL
Dosage Form : TABLET;ORAL
Dosage Strength : 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 12703
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ELAVIL
Dosage Form : TABLET;ORAL
Dosage Strength : 150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 12703
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ELAVIL
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 10MG/ML
Packaging :
Approval Date : 1982-01-01
Application Number : 12704
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 : RX
Registration Country : USA
Brand Name : AMITRIPTYLINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG
Packaging :
Approval Date : 2021-02-19
Application Number : 213999
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : AMITRIPTYLINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 25MG
Packaging :
Approval Date : 2021-02-19
Application Number : 213999
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : AMITRIPTYLINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 50MG
Packaging :
Approval Date : 2021-02-19
Application Number : 213999
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : AMITRIPTYLINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 75MG
Packaging :
Approval Date : 2021-02-19
Application Number : 213999
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : AMITRIPTYLINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 100MG
Packaging :
Approval Date : 2021-02-19
Application Number : 213999
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : AMITRIPTYLINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 150MG
Packaging :
Approval Date : 2021-02-19
Application Number : 213999
Regulatory Info : RX
Registration Country : USA
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