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01 2DR REDDYS LABS SA

02 4ACTAVIS LABS FL INC

03 2AEGIS PHARMS

04 2APOTEX

05 2ASTRAZENECA

06 2EUGIA PHARMA

07 2IVAX SUB TEVA PHARMS

08 1MAYNE PHARMA COMMRCL

09 2MYLAN

10 1PHARMACHEMIE

11 2ROXANE

12 2TEVA

13 2ZYDUS PHARMS

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

RLD : No

TE Code : AB

TAMOXIFEN CITRATE

Brand Name : TAMOXIFEN CITRATE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 10MG BASE

Approval Date : 2003-02-20

Application Number : 75797

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Dr Reddy Company Banner

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

RLD : No

TE Code : AB

TAMOXIFEN CITRATE

Brand Name : TAMOXIFEN CITRATE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 20MG BASE

Approval Date : 2003-02-20

Application Number : 75797

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Dr Reddy Company Banner

03

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

TAMOXIFEN CITRATE

Brand Name : TAMOXIFEN CITRATE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 10MG BASE

Approval Date : 2003-02-20

Application Number : 70929

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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04

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

TAMOXIFEN CITRATE

Brand Name : TAMOXIFEN CITRATE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 20MG BASE

Approval Date : 2003-02-20

Application Number : 70929

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

blank

05

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

TAMOXIFEN CITRATE

Brand Name : NOLVADEX

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 17970

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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06

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

TAMOXIFEN CITRATE

Brand Name : NOLVADEX

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 20MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1994-03-21

Application Number : 17970

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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07

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

TAMOXIFEN CITRATE

Brand Name : SOLTAMOX

Dosage Form : SOLUTION;ORAL

Dosage Strength : EQ 20MG BASE/10ML

Approval Date : 2005-10-29

Application Number : 21807

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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08

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

TAMOXIFEN CITRATE

Brand Name : TAMOXIFEN CITRATE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 10MG BASE

Approval Date : 2003-03-31

Application Number : 74539

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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09

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

TAMOXIFEN CITRATE

Brand Name : TAMOXIFEN CITRATE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 10MG BASE

Approval Date : 2003-04-28

Application Number : 74504

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank

10

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

TAMOXIFEN CITRATE

Brand Name : TAMOXIFEN CITRATE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 20MG BASE

Approval Date : 2003-04-28

Application Number : 74504

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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