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01 5ACCORD HLTHCARE

02 4ACTAVIS TOTOWA

03 3CIPLA LTD

04 3CORDEN PHARMA

05 4CORDENPHARMA

06 4EPIC PHARMA LLC

07 4EUGIA PHARMA

08 13FRESENIUS KABI USA

09 4GLAND PHARMA LTD

10 7HIKMA

11 7HOSPIRA

12 4MEITHEAL

13 3NATCO PHARMA USA

14 8NORVIUM BIOSCIENCE

15 4NOVAST LABS

16 7PHARMACHEMIE BV

17 3PLIVA

18 4PLIVA LACHEMA

19 6SANDOZ

20 3SUN PHARM

21 3TEVA PARENTERAL

22 4TEVA PHARMS USA

23 4TEYRO LABS

24 3WATSON LABS TEVA

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PharmaCompass

01

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
Not Confirmed

CARBOPLATIN

Brand Name : PARAPLATIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 50MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1989-03-03

Application Number : 19880

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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02

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
Not Confirmed

CARBOPLATIN

Brand Name : PARAPLATIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 150MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1989-03-03

Application Number : 19880

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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03

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
Not Confirmed

CARBOPLATIN

Brand Name : PARAPLATIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 450MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1989-03-03

Application Number : 19880

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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04

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
Not Confirmed

CARBOPLATIN

Brand Name : PARAPLATIN

Dosage Form : INJECTABLE;INTRAVENOUS

Dosage Strength : 50MG/5ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 2003-07-14

Application Number : 20452

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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05

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
Not Confirmed

CARBOPLATIN

Brand Name : PARAPLATIN

Dosage Form : INJECTABLE;INTRAVENOUS

Dosage Strength : 150MG/15ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 2003-07-14

Application Number : 20452

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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06

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
Not Confirmed

CARBOPLATIN

Brand Name : PARAPLATIN

Dosage Form : INJECTABLE;INTRAVENOUS

Dosage Strength : 450MG/45ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 2003-07-14

Application Number : 20452

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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07

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
Not Confirmed

CARBOPLATIN

Brand Name : PARAPLATIN

Dosage Form : INJECTABLE;INTRAVENOUS

Dosage Strength : 600MG/60ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 2004-01-15

Application Number : 20452

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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08

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
Not Confirmed

CARBOPLATIN

Brand Name : CARBOPLATIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 50MG/VIAL

Approval Date : 2004-10-14

Application Number : 76099

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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09

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
Not Confirmed

CARBOPLATIN

Brand Name : CARBOPLATIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 150MG/VIAL

Approval Date : 2004-10-14

Application Number : 76099

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank

10

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
Not Confirmed

CARBOPLATIN

Brand Name : CARBOPLATIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 450MG/VIAL

Approval Date : 2004-10-14

Application Number : 76099

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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