Please Wait
Applying Filters...
Menu
$ API Ref.Price (USD/KG) : 1,449Xls
Filters Filter
Cross PopUp
FILTER :

filter clear-filterReset all filters

01 10ABRAXIS PHARM

02 4Abbott Laboratories

03 4Actavis Inc

04 2Amneal Pharmaceuticals

05 4Amphastar Pharmaceuticals

06 4Aurobindo Pharma Limited

07 6BEDFORD LABS

08 2Bharat Parenterals Limited

09 2Chongqing Huapont Pharmaceutical

10 4ELKINS SINN

11 1East African (India) Overseas

12 3Flagship Biotech International Pvt. Ltd

13 3Fresenius Kabi USA

14 4Health Biotech

15 4Hikma Pharmaceuticals

16 10Hospira, Inc.

17 3Lisapharma Spa

18 2Merck & Co

19 1Modern Laboratories

20 4Montage Laboratories

21 11Pfizer Inc

22 3Polifarma

23 4Quad Pharma

24 5Sagent Pharmaceuticals

25 3Teva Pharmaceutical Industries

26 5Tianjin Tianfa Pharmaceutical Import & Export

filter clear-filterReset all filters

filter clear-filterReset all filters

filter clear-filterReset all filters

filter clear-filterReset all filters

PharmaCompass

01

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

METHYLPREDNISOLONE SODIUM SUCCINATE

Brand Name : METHYLPREDNISOLONE SODIUM SUCCINATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 125MG BASE/VIAL

Packaging :

Approval Date : 2007-02-21

Application Number : 40641

Regulatory Info : DISCN

Registration Country : USA

blank

02

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

METHYLPREDNISOLONE SODIUM SUCCINATE

Brand Name : METHYLPREDNISOLONE SODIUM SUCCINATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 500MG BASE/VIAL

Packaging :

Approval Date : 2007-02-21

Application Number : 40641

Regulatory Info : DISCN

Registration Country : USA

blank

03

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

METHYLPREDNISOLONE SODIUM SUCCINATE

Brand Name : METHYLPREDNISOLONE SODIUM SUCCINATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1GM BASE/VIAL

Packaging :

Approval Date : 2007-02-21

Application Number : 40641

Regulatory Info : DISCN

Registration Country : USA

blank

04

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

METHYLPREDNISOLONE SODIUM SUCCINATE

Brand Name : METHYLPREDNISOLONE SODIUM SUCCINATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 40MG BASE/VIAL

Packaging :

Approval Date : 2007-02-21

Application Number : 40662

Regulatory Info : DISCN

Registration Country : USA

blank

05

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

METHYLPREDNISOLONE SODIUM SUCCINATE

Brand Name : METHYLPREDNISOLONE SODIUM SUCCINATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 500MG BASE/VIAL

Packaging :

Approval Date : 2007-02-21

Application Number : 40709

Regulatory Info : DISCN

Registration Country : USA

blank

06

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

METHYLPREDNISOLONE SODIUM SUCCINATE

Brand Name : METHYLPREDNISOLONE SODIUM SUCCINATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1GM BASE/VIAL

Packaging :

Approval Date : 2007-02-21

Application Number : 40709

Regulatory Info : DISCN

Registration Country : USA

blank

07

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

METHYLPREDNISOLONE SODIUM SUCCINATE

Brand Name : METHYLPREDNISOLONE SODIUM SUCCINATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 40MG BASE/VIAL

Packaging :

Approval Date : 2004-07-30

Application Number : 40583

Regulatory Info : RX

Registration Country : USA

blank

08

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

METHYLPREDNISOLONE SODIUM SUCCINATE

Brand Name : METHYLPREDNISOLONE SODIUM SUCCINATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 125MG BASE/VIAL

Packaging :

Approval Date : 2004-07-30

Application Number : 40583

Regulatory Info : RX

Registration Country : USA

blank

09

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

METHYLPREDNISOLONE SODIUM SUCCINATE

Brand Name : METHYLPREDNISOLONE SODIUM SUCCINATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1GM BASE/VIAL

Packaging :

Approval Date : 2004-08-12

Application Number : 40612

Regulatory Info : RX

Registration Country : USA

blank

10

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

METHYLPREDNISOLONE SODIUM SUCCINATE

Brand Name : A-METHAPRED

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 40MG BASE/VIAL

Packaging :

Approval Date : 2005-12-20

Application Number : 40664

Regulatory Info : DISCN

Registration Country : USA

blank

11

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

METHYLPREDNISOLONE SODIUM SUCCINATE

Brand Name : A-METHAPRED

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 125MG BASE/VIAL

Packaging :

Approval Date : 2005-12-20

Application Number : 40665

Regulatory Info : DISCN

Registration Country : USA

blank

12

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

METHYLPREDNISOLONE SODIUM SUCCINATE

Brand Name : A-METHAPRED

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 40MG BASE/VIAL

Packaging :

Approval Date : 2008-11-25

Application Number : 40793

Regulatory Info : DISCN

Registration Country : USA

blank

13

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

METHYLPREDNISOLONE SODIUM SUCCINATE

Brand Name : A-METHAPRED

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 125MG BASE/VIAL

Packaging :

Approval Date : 2008-11-25

Application Number : 40827

Regulatory Info : DISCN

Registration Country : USA

blank

14

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

METHYLPREDNISOLONE SODIUM SUCCINATE

Brand Name : SOLU-MEDROL

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 40MG BASE/VIAL

Packaging :

Approval Date : 1982-01-01

Application Number : 11856

Regulatory Info : RX

Registration Country : USA

blank

15

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

METHYLPREDNISOLONE SODIUM SUCCINATE

Brand Name : SOLU-MEDROL

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 125MG BASE/VIAL

Packaging :

Approval Date : 1982-01-01

Application Number : 11856

Regulatory Info : RX

Registration Country : USA

blank

16

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

METHYLPREDNISOLONE SODIUM SUCCINATE

Brand Name : SOLU-MEDROL

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 500MG BASE/VIAL

Packaging :

Approval Date : 1982-01-01

Application Number : 11856

Regulatory Info : RX

Registration Country : USA

blank

17

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

METHYLPREDNISOLONE SODIUM SUCCINATE

Brand Name : SOLU-MEDROL

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1GM BASE/VIAL

Packaging :

Approval Date : 1982-01-01

Application Number : 11856

Regulatory Info : RX

Registration Country : USA

blank

18

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

METHYLPREDNISOLONE SODIUM SUCCINATE

Brand Name : SOLU-MEDROL

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 2GM BASE/VIAL

Packaging :

Approval Date : 1985-02-27

Application Number : 11856

Regulatory Info : RX

Registration Country : USA

blank

19

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

METHYLPREDNISOLONE SODIUM SUCCINATE

Brand Name : METHYLPREDNISOLONE SODIUM SUCCINATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 40MG BASE/VIAL

Packaging :

Approval Date : 2011-07-18

Application Number : 40888

Regulatory Info : RX

Registration Country : USA

blank

20

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

METHYLPREDNISOLONE SODIUM SUCCINATE

Brand Name : METHYLPREDNISOLONE SODIUM SUCCINATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 125MG BASE/VIAL

Packaging :

Approval Date : 2011-07-18

Application Number : 40888

Regulatory Info : RX

Registration Country : USA

blank