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
01 27INJECTABLE;INJECTION
02 87INJECTABLE;INTRAVENOUS
01 68DISCN
02 46RX
01 107CARBOPLATIN
02 7PARAPLATIN
01 107No
02 7Yes
RLD : Yes
TE Code :
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Dosage Strength : 50MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 :
RLD : Yes
TE Code :
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Dosage Strength : 150MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 :
RLD : Yes
TE Code :
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Dosage Strength : 450MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 :
RLD : Yes
TE Code :
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Dosage Strength : 50MG/5ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 :
RLD : Yes
TE Code :
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Dosage Strength : 150MG/15ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 :
RLD : Yes
TE Code :
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Dosage Strength : 450MG/45ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 :
RLD : Yes
TE Code :
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 :
RLD : No
TE Code :
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 :
RLD : No
TE Code :
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 :
RLD : No
TE Code :
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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