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01 6BRECKENRIDGE

02 6ACCORD HLTHCARE

03 6AIPING PHARM INC

04 4AM THERAP

05 2ANDA REPOSITORY

06 4ANI PHARMS

07 1ANI PHARMS INC

08 7ASTRAZENECA

09 6AUROBINDO PHARMA USA

10 5BRISTOL MYERS SQUIBB

11 8CHARTWELL RX

12 6COPLEY PHARM

13 6ENDO OPERATIONS

14 5FOSUN PHARMA

15 6HALSEY

16 2HERITAGE PHARMA

17 5IVAX SUB TEVA PHARMS

18 11LEDERLE

19 6MANKIND PHARMA

20 2MICRO LABS

21 8MUTUAL PHARM

22 15MYLAN

23 2MYLAN PHARMS INC

24 5NEW RIVER

25 11PAR PHARM

26 6PLIVA

27 10PUREPAC PHARM

28 6RISING

29 7ROCHE

30 12ROXANE

31 6RUBICON

32 7SANDOZ

33 4SCHERING

34 12SUN PHARM INDS INC

35 4SUN PHARM INDUSTRIES

36 5SUPERPHARM

37 7TEVA

38 6UCB INC

39 6UNICHEM

40 3USL PHARMA

41 4VANGARD

42 6WARNER CHILCOTT

43 24WATSON LABS

44 2WEST WARD

45 6ZYDUS PHARMS

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PharmaCompass

01

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Pharmtech & Ingredients
Not Confirmed

AMITRIPTYLINE HYDROCHLORIDE

Brand Name : AMITRIPTYLINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG

Approval Date : 2022-06-06

Application Number : 216243

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Breckenridge Pharmaceutical

02

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Pharmtech & Ingredients
Not Confirmed

AMITRIPTYLINE HYDROCHLORIDE

Brand Name : AMITRIPTYLINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 25MG

Approval Date : 2022-06-06

Application Number : 216243

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Breckenridge Pharmaceutical

03

arrow
Pharmtech & Ingredients
Not Confirmed

AMITRIPTYLINE HYDROCHLORIDE

Brand Name : AMITRIPTYLINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 50MG

Approval Date : 2022-06-06

Application Number : 216243

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Breckenridge Pharmaceutical

04

arrow
Pharmtech & Ingredients
Not Confirmed

AMITRIPTYLINE HYDROCHLORIDE

Brand Name : AMITRIPTYLINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 75MG

Approval Date : 2022-06-06

Application Number : 216243

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Breckenridge Pharmaceutical

05

arrow
Pharmtech & Ingredients
Not Confirmed

AMITRIPTYLINE HYDROCHLORIDE

Brand Name : AMITRIPTYLINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 100MG

Approval Date : 2022-06-06

Application Number : 216243

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Breckenridge Pharmaceutical

06

arrow
Pharmtech & Ingredients
Not Confirmed

AMITRIPTYLINE HYDROCHLORIDE

Brand Name : AMITRIPTYLINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 150MG

Approval Date : 2022-06-06

Application Number : 216243

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Breckenridge Pharmaceutical

07

Pharmtech & Ingredients
Not Confirmed
arrow
arrow
Pharmtech & Ingredients
Not Confirmed

AMITRIPTYLINE HYDROCHLORIDE

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**

Approval Date : 1982-01-01

Application Number : 12703

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank

08

Pharmtech & Ingredients
Not Confirmed
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arrow
Pharmtech & Ingredients
Not Confirmed

AMITRIPTYLINE HYDROCHLORIDE

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**

Approval Date : 1982-01-01

Application Number : 12703

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank

09

Pharmtech & Ingredients
Not Confirmed
arrow
arrow
Pharmtech & Ingredients
Not Confirmed

AMITRIPTYLINE HYDROCHLORIDE

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**

Approval Date : 1982-01-01

Application Number : 12703

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank

10

Pharmtech & Ingredients
Not Confirmed
arrow
arrow
Pharmtech & Ingredients
Not Confirmed

AMITRIPTYLINE HYDROCHLORIDE

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**

Approval Date : 1982-01-01

Application Number : 12703

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank