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01 10ABBVIE

02 1ALLERGAN

03 2STRIDES PHARMA

04 2ACME LABS

05 2AJANTA PHARMA LTD

06 2ALEMBIC

07 2ALLIED

08 8AMNEAL PHARMS

09 5ANI PHARMS

10 5APOTEX

11 6AUROBINDO PHARMA LTD

12 2CHARTWELL

13 1CHARTWELL MOLECULAR

14 2DR REDDYS LABS LTD

15 4ENDO OPERATIONS

16 2HETERO LABS LTD V

17 2HIKMA

18 2JUBILANT GENERICS

19 2LANNETT CO INC

20 6LUPIN LTD

21 7MACLEODS PHARMS LTD

22 4NOVAST LABS LTD

23 2ORBION PHARMS

24 2POLYGEN PHARMS

25 2PURACAP PHARM LLC

26 6RISING

27 1SCIEGEN PHARMS INC

28 1SETON PHARMS

29 6SUN PHARM

30 2TEVA PHARMS

31 2TORRENT

32 2UNICHEM

33 2UPSHER SMITH LABS

34 6XIAMEN LP PHARM CO

35 4YICHANG HUMANWELL

36 2YILING

37 2ZYDUS LIFESCIENCES

38 4ZYDUS PHARMS

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PharmaCompass

01

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Pharmtech & Ingredients
Not Confirmed

MEMANTINE HYDROCHLORIDE

Brand Name : NAMENDA

Dosage Form : TABLET;ORAL

Dosage Strength : 5MG

Approval Date : 2003-10-16

Application Number : 21487

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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02

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Pharmtech & Ingredients
Not Confirmed

MEMANTINE HYDROCHLORIDE

Brand Name : NAMENDA

Dosage Form : SOLUTION;ORAL

Dosage Strength : 2MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 2005-04-18

Application Number : 21627

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

Abbvie CB

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothStrides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.

RLD : No

TE Code : AB

MEMANTINE HYDROCHLORIDE

Brand Name : MEMANTINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 5MG

Approval Date : 2017-05-23

Application Number : 202350

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Strides Pharma Science

04

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Pharmtech & Ingredients
Not Confirmed

MEMANTINE HYDROCHLORIDE

Brand Name : NAMENDA

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG

Approval Date : 2003-10-16

Application Number : 21487

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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05

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Pharmtech & Ingredients
Not Confirmed

MEMANTINE HYDROCHLORIDE

Brand Name : NAMENDA XR

Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

Dosage Strength : 7MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 2010-06-21

Application Number : 22525

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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06

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Pharmtech & Ingredients
Not Confirmed

MEMANTINE HYDROCHLORIDE

Brand Name : NAMENDA XR

Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

Dosage Strength : 14MG

Approval Date : 2010-06-21

Application Number : 22525

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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07

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Pharmtech & Ingredients
Not Confirmed

MEMANTINE HYDROCHLORIDE

Brand Name : NAMENDA XR

Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

Dosage Strength : 21MG

Approval Date : 2010-06-21

Application Number : 22525

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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08

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Pharmtech & Ingredients
Not Confirmed

MEMANTINE HYDROCHLORIDE

Brand Name : NAMENDA XR

Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

Dosage Strength : 28MG

Approval Date : 2010-06-21

Application Number : 22525

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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09

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Pharmtech & Ingredients
Not Confirmed

DONEPEZIL HYDROCHLORIDE; MEMANTINE HYDROCHLORIDE

Brand Name : NAMZARIC

Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

Dosage Strength : 10MG;14MG

Approval Date : 2014-12-23

Application Number : 206439

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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10

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Pharmtech & Ingredients
Not Confirmed

DONEPEZIL HYDROCHLORIDE; MEMANTINE HYDROCHLORIDE

Brand Name : NAMZARIC

Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

Dosage Strength : 10MG;28MG

Approval Date : 2014-12-23

Application Number : 206439

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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