loader
Please Wait
Applying Filters...

Approved Drug Products containing preventative factor listed in the FDA Orange Book. Original Data : FDA Website

Menu
$ API Ref.Price (USD/KG) : 6Xls
Filters Filter
Cross PopUp
FILTER :

filter clear-filterReset all filters

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

filter clear-filterReset all filters

filter clear-filterReset all filters

filter clear-filterReset all filters

filter clear-filterReset all filters

PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

RLD : Yes

TE Code :

NIACIN

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 :

Sanofi Company Banner

02

arrow
BioProcess International
Not Confirmed

NIACIN

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 :

Abbvie Company Banner

03

arrow
BioProcess International
Not Confirmed

NIACIN

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Dosage Strength : 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 :

Abbvie Company Banner

04

arrow
BioProcess International
Not Confirmed

NIACIN

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Dosage Strength : 750MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 :

Abbvie Company Banner

05

arrow
BioProcess International
Not Confirmed

NIACIN

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 :

Abbvie Company Banner

06

arrow
BioProcess International
Not Confirmed

NIACIN

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 :

Abbvie Company Banner

07

BioProcess International
Not Confirmed
arrow
arrow
BioProcess International
Not Confirmed

NIACIN

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 :

blank

08

BioProcess International
Not Confirmed
arrow
arrow
BioProcess International
Not Confirmed

NIACIN

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

blank

09

BioProcess International
Not Confirmed
arrow
arrow
BioProcess International
Not Confirmed

NIACIN

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

blank

10

BioProcess International
Not Confirmed
arrow
arrow
BioProcess International
Not Confirmed

NIACIN

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 :

blank