Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
01 2SANOFI AVENTIS US
02 3AUROBINDO PHARMA
03 1AUROBINDO PHARMA LTD
04 2B BRAUN
05 1CEPHAZONE PHARMA
06 5FRESENIUS KABI USA
07 4HIKMA
08 2HOSPIRA
09 6HOSPIRA INC
10 3LUPIN
11 8STERIMAX
12 3WOCKHARDT
01 40INJECTABLE;INJECTION
01 40DISCN
01 10CEFOTAXIME
02 1CEFOTAXIME AND DEXTROSE 2.4% IN PLASTIC CONTAINER
03 1CEFOTAXIME AND DEXTROSE 3.9% IN PLASTIC CONTAINER
04 18CEFOTAXIME SODIUM
05 6CLAFORAN
06 2CLAFORAN IN DEXTROSE 5% IN PLASTIC CONTAINER
07 2CLAFORAN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
01 36No
02 4Yes
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
RLD : No
TE Code :
Brand Name : CLAFORAN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1GM BASE/VIAL
Approval Date : 1987-01-13
Application Number : 62659
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
RLD : No
TE Code :
Brand Name : CLAFORAN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 2GM BASE/VIAL
Approval Date : 1987-01-13
Application Number : 62659
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
Brand Name : CLAFORAN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 50547
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : CLAFORAN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 50547
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : CLAFORAN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 2GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 50547
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : CLAFORAN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 10GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1983-12-29
Application Number : 50547
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
Brand Name : CLAFORAN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 20MG BASE/ML
Approval Date : 1985-05-20
Application Number : 50596
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : CLAFORAN IN DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 20MG BASE/ML
Approval Date : 1985-05-20
Application Number : 50596
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : CLAFORAN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 40MG BASE/ML
Approval Date : 1985-05-20
Application Number : 50596
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : CLAFORAN IN DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 40MG BASE/ML
Approval Date : 1985-05-20
Application Number : 50596
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
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