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01 6ABBVIE

02 2ABBVIE INC

03 1DR REDDYS LABS SA

04 1ACTAVIS LABS FL INC

05 2ALEMBIC

06 2ANI PHARMS

07 2AUROBINDO

08 2CHARTWELL

09 1CUMBERLAND

10 2ESJAY PHARMA

11 2HEC PHARM

12 2HIKMA

13 2IVAX SUB TEVA PHARMS

14 2JUBILANT CADISTA

15 1LUPIN LTD

16 2NORVIUM BIOSCIENCE

17 1NOSTRUM LABS INC

18 1RANBAXY

19 1RISING

20 5SANDOZ

21 4SUN PHARM INDS LTD

22 1SUNSHINE

23 1TAKEDA PHARMS USA

24 2TEVA

25 2WOCKHARDT

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PharmaCompass

01

CLARITHROMYCIN

Brand Name : BIAXIN

Dosage Form : TABLET;ORAL

Dosage Strength : 250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1991-10-31

Application Number : 50662

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

Abbvie 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

CLARITHROMYCIN

Brand Name : CLARITHROMYCIN

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : 500MG

Approval Date : 2005-05-18

Application Number : 65154

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Dr Reddy Company Banner

03

CLARITHROMYCIN

Brand Name : BIAXIN

Dosage Form : TABLET;ORAL

Dosage Strength : 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1991-10-31

Application Number : 50662

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

Abbvie Company Banner

09

CLARITHROMYCIN

Brand Name : BIAXIN XL

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 2000-03-03

Application Number : 50775

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

Abbvie Company Banner

10

Europ. Pharma Outsourcing
Not Confirmed
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Europ. Pharma Outsourcing
Not Confirmed

AMOXICILLIN; CLARITHROMYCIN; LANSOPRAZOLE

Brand Name : PREVPAC (COPACKAGED)

Dosage Form : CAPSULE, TABLET, CAPSULE, DELAYED REL PELLETS;ORAL

Dosage Strength : 500MG;500MG;30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1997-12-02

Application Number : 50757

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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