01 5ACCORD HLTHCARE
02 4ACTAVIS TOTOWA
03 3AVYXA HOLDINGS
04 3CIPLA LTD
05 3CORDEN PHARMA
06 4CORDENPHARMA
07 4EPIC PHARMA LLC
08 4EUGIA PHARMA
09 13FRESENIUS KABI USA
10 4GLAND
11 7HIKMA
12 7HOSPIRA
13 4MEITHEAL
14 3NATCO PHARMA USA
15 4NOVAST LABS
16 7PHARMACHEMIE BV
17 8PHARMOBEDIENT
18 3PLIVA
19 4PLIVA LACHEMA
20 6SANDOZ
21 3SUN PHARM
22 3TEVA PARENTERAL
23 4TEVA PHARMS USA
24 4TEYRO LABS
25 3WATSON LABS TEVA
01 27INJECTABLE;INJECTION
02 87INJECTABLE;INTRAVENOUS
03 3SOLUTION;INTRAVENOUS
01 68DISCN
02 46RX
03 3Blank
01 107CARBOPLATIN
02 3KYXATA
03 7PARAPLATIN
01 107No
02 7Yes
03 3Blank
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Dosage Strength : 50MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : 150MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : 450MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : 50MG/5ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : 150MG/15ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : 450MG/45ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 :
