Please Wait
Applying Filters...
Menu
$ API Ref.Price (USD/KG) : 303Xls
Filters Filter
Cross PopUp
FILTER :

filter clear-filterReset all filters

01 1GRANULES

02 1ACTAVIS LABS FL INC

03 1ANDA REPOSITORY

04 1APOTEX INC

05 1AUROBINDO PHARMA

06 3AUROBINDO PHARMA LTD

07 12BAYER HEALTHCARE LLC

08 2BIONPHARMA

09 1CATALENT PHARMA

10 1FDN CONSUMER

11 1GLAXOSMITHKLINE

12 1HERITAGE PHARMA

13 1HETERO LABS LTD III

14 1HETERO LABS LTD V

15 1LANNETT CO INC

16 2MARKSANS PHARMA

17 1MYLAN

18 2NORVIUM BIOSCIENCE

19 1P AND L

20 3PERRIGO

21 4PERRIGO PHARMA INTL

22 2PHARM ASSOC

23 1PLD ACQUISITIONS LLC

24 1RANBAXY LABS LTD

25 1RUBICON

26 1STRIDES SOFTGELS

27 1SUN PHARM

28 3SUN PHARM INDS LTD

29 3TARO

30 2TENSHI

31 1TEVA

32 1UNIQUE PHARM

33 1WOCKHARDT BIO AG

filter clear-filterReset all filters

filter clear-filterReset all filters

filter clear-filterReset all filters

filter clear-filterReset all filters

PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothGranules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.

RLD : No

TE Code :

LORATADINE

Brand Name : LORATADINE

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG

Approval Date : 2019-12-23

Application Number : 210722

RX/OTC/DISCN : OTC

RLD : No

TE Code :

Granules India

02

German Wound Congress
Not Confirmed
arrow
arrow
German Wound Congress
Not Confirmed

LORATADINE

Brand Name : CLARITIN

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG

Approval Date : 2002-11-27

Application Number : 19658

RX/OTC/DISCN : OTC

RLD : Yes

TE Code :

blank

03

German Wound Congress
Not Confirmed
arrow
arrow
German Wound Congress
Not Confirmed

LORATADINE

Brand Name : CLARITIN HIVES RELIEF

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG

Approval Date : 2003-11-19

Application Number : 19658

RX/OTC/DISCN : OTC

RLD : Yes

TE Code :

blank

04

German Wound Congress
Not Confirmed
arrow
arrow
German Wound Congress
Not Confirmed

LORATADINE; PSEUDOEPHEDRINE SULFATE

Brand Name : CLARITIN-D

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : 5MG;120MG

Approval Date : 2002-11-27

Application Number : 19670

RX/OTC/DISCN : OTC

RLD : Yes

TE Code :

blank

05

German Wound Congress
Not Confirmed
arrow
arrow
German Wound Congress
Not Confirmed

LORATADINE; PSEUDOEPHEDRINE SULFATE

Brand Name : CLARITIN-D 24 HOUR

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : 10MG;240MG

Approval Date : 2002-11-27

Application Number : 20470

RX/OTC/DISCN : OTC

RLD : Yes

TE Code :

blank

06

German Wound Congress
Not Confirmed
arrow
arrow
German Wound Congress
Not Confirmed

LORATADINE

Brand Name : CLARITIN

Dosage Form : SYRUP;ORAL

Dosage Strength : 1MG/ML

Approval Date : 2002-11-27

Application Number : 20641

RX/OTC/DISCN : OTC

RLD : Yes

TE Code :

blank

07

German Wound Congress
Not Confirmed
arrow
arrow
German Wound Congress
Not Confirmed

LORATADINE

Brand Name : CLARITIN HIVES RELIEF

Dosage Form : SYRUP;ORAL

Dosage Strength : 1MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 2003-11-19

Application Number : 20641

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank

08

German Wound Congress
Not Confirmed
arrow
arrow
German Wound Congress
Not Confirmed

LORATADINE

Brand Name : CLARITIN REDITABS

Dosage Form : TABLET, ORALLY DISINTEGRATING;ORAL

Dosage Strength : 10MG

Approval Date : 2002-11-27

Application Number : 20704

RX/OTC/DISCN : OTC

RLD : Yes

TE Code :

blank

09

German Wound Congress
Not Confirmed
arrow
arrow
German Wound Congress
Not Confirmed

LORATADINE

Brand Name : CLARITIN HIVES RELIEF REDITAB

Dosage Form : TABLET, ORALLY DISINTEGRATING;ORAL

Dosage Strength : 10MG

Approval Date : 2003-11-19

Application Number : 20704

RX/OTC/DISCN : OTC

RLD : Yes

TE Code :

blank

10

German Wound Congress
Not Confirmed
arrow
arrow
German Wound Congress
Not Confirmed

LORATADINE

Brand Name : ALAVERT

Dosage Form : TABLET, ORALLY DISINTEGRATING;ORAL

Dosage Strength : 10MG

Approval Date : 2002-12-19

Application Number : 21375

RX/OTC/DISCN : OTC

RLD : No

TE Code :

blank