Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
01 1SANOFI AVENTIS US
02 5ABBVIE
03 3AMNEAL PHARMS
04 3AUROBINDO PHARMA LTD
05 1AVONDALE PHARMS
06 3BARR
07 2BEIJING
08 3CHARTWELL RX
09 1EVERYLIFE
10 1HALSEY
11 3HIBROW HLTHCARE
12 1HIKMA
13 1IMPAX LABS
14 1IVAX SUB TEVA PHARMS
15 3JUBILANT GENERICS
16 2LANNETT CO INC
17 2MACLEODS PHARMS LTD
18 1MEDPOINTE PHARM HLC
19 1MK LABS
20 1PUREPAC PHARM
21 3RISING
22 1SANDOZ
23 3SUN PHARM
24 1TABLICAPS
25 3WATSON LABS
26 1WOCKHARDT
27 3YICHANG HUMANWELL
01 1CAPSULE;ORAL
02 38TABLET, EXTENDED RELEASE;ORAL
03 15TABLET;ORAL
01 31DISCN
02 23RX
01 46NIACIN
02 1NIACOR
03 4NIASPAN
04 1NIASPAN TITRATION STARTER PACK
05 1NICOLAR
06 1WAMPOCAP
01 50No
02 4Yes
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
RLD : Yes
TE Code :
Brand Name : NICOLAR
Dosage Form : TABLET;ORAL
Dosage Strength : 500MG
Approval Date : 1982-01-01
Application Number : 83823
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
Brand Name : NIASPAN
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 375MG
Approval Date : 1997-07-28
Application Number : 20381
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
Brand Name : NIASPAN
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1997-07-28
Application Number : 20381
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : NIASPAN
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 750MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1997-07-28
Application Number : 20381
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : NIASPAN
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 1GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1997-07-28
Application Number : 20381
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
Brand Name : NIASPAN TITRATION STARTER PACK
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 375MG;500MG;750MG
Approval Date : 1997-07-28
Application Number : 20381
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : NIACOR
Dosage Form : TABLET;ORAL
Dosage Strength : 500MG
Approval Date : 2000-05-03
Application Number : 40378
RX/OTC/DISCN : RX
RLD : No
TE Code :
RLD : No
TE Code : AB
Brand Name : NIACIN
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 1GM
Approval Date : 2005-04-14
Application Number : 76250
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : NIACIN
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 500MG
Approval Date : 2005-04-26
Application Number : 76378
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code :
Brand Name : WAMPOCAP
Dosage Form : CAPSULE;ORAL
Dosage Strength : 500MG
Approval Date : 1982-01-01
Application Number : 11073
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
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