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01 3AMNEAL PHARMS

02 1AUROBINDO PHARMA

03 2AUROBINDO PHARMA LTD

04 3BARR

05 1BARR LABS INC

06 2ENDO OPERATIONS

07 2GLENMARK PHARMS LTD

08 1GLENMARK SPECLT

09 5JANSSEN PHARMS

10 2LUPIN LTD

11 1LUPIN PHARMS

12 1MYLAN

13 2NAARI PTE LTD

14 1NOVAST LABS

15 2NOVAST LABS LTD

16 2ORTHO MCNEIL PHARM

17 1TEVA WOMENS

18 3WATSON LABS

19 5XIROMED

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PharmaCompass

01

Antibody Engineering
Not Confirmed
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Antibody Engineering
Not Confirmed

ETHINYL ESTRADIOL; NORGESTIMATE

Brand Name : SPRINTEC

Dosage Form : TABLET;ORAL-28

Dosage Strength : 0.035MG;0.25MG

Approval Date : 2002-09-25

Application Number : 75804

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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02

Antibody Engineering
Not Confirmed
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Antibody Engineering
Not Confirmed

ETHINYL ESTRADIOL; NORGESTIMATE

Brand Name : TRI-SPRINTEC

Dosage Form : TABLET;ORAL-28

Dosage Strength : 0.035MG,0.035MG,0.035MG;0.18MG,0.215MG,0.25MG

Approval Date : 2003-12-29

Application Number : 75808

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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03

Antibody Engineering
Not Confirmed
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Antibody Engineering
Not Confirmed

ETHINYL ESTRADIOL; NORGESTIMATE

Brand Name : ORTHO CYCLEN-21

Dosage Form : TABLET;ORAL-21

Dosage Strength : 0.035MG;0.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1989-12-29

Application Number : 19653

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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04

Antibody Engineering
Not Confirmed
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Antibody Engineering
Not Confirmed

ETHINYL ESTRADIOL; NORGESTIMATE

Brand Name : ORTHO CYCLEN-28

Dosage Form : TABLET;ORAL-28

Dosage Strength : 0.035MG;0.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1989-12-29

Application Number : 19653

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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05

Antibody Engineering
Not Confirmed
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Antibody Engineering
Not Confirmed

ETHINYL ESTRADIOL; NORGESTIMATE

Brand Name : ORTHO TRI-CYCLEN

Dosage Form : TABLET;ORAL-28

Dosage Strength : 0.035MG,0.035MG,0.035MG;0.18MG,0.215MG,0.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1992-07-03

Application Number : 19697

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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06

Antibody Engineering
Not Confirmed
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Antibody Engineering
Not Confirmed

ETHINYL ESTRADIOL; NORGESTIMATE

Brand Name : ORTHO TRI-CYCLEN

Dosage Form : TABLET;ORAL-21

Dosage Strength : 0.035MG,0.035MG,0.035MG;0.18MG,0.215MG,0.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1992-07-03

Application Number : 19697

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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07

Antibody Engineering
Not Confirmed
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Antibody Engineering
Not Confirmed

ETHINYL ESTRADIOL; NORGESTIMATE

Brand Name : ORTHO TRI-CYCLEN LO

Dosage Form : TABLET;ORAL-28

Dosage Strength : 0.025MG,0.025MG,0.025MG;0.18MG,0.215MG,0.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 2002-08-22

Application Number : 21241

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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08

Antibody Engineering
Not Confirmed
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Antibody Engineering
Not Confirmed

ETHINYL ESTRADIOL; NORGESTIMATE

Brand Name : ORTHO TRI-CYCLEN 21

Dosage Form : TABLET; ORAL-21

Dosage Strength : 0.035MG,0.035MG,0.035MG; 0.18MG,0.215MG,0.25MG

Approval Date :

Application Number : 21690

RX/OTC/DISCN :

RLD :

TE Code :

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09

Antibody Engineering
Not Confirmed
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Antibody Engineering
Not Confirmed

ETHINYL ESTRADIOL; NORGESTIMATE

Brand Name : ORTHO TRI-CYCLEN 28

Dosage Form : TABLET; ORAL-28

Dosage Strength : 0.035MG,0.035MG,0.035MG; 0.18MG,0.215MG,0.25MG

Approval Date :

Application Number : 21690

RX/OTC/DISCN :

RLD :

TE Code :

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10

Antibody Engineering
Not Confirmed
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Antibody Engineering
Not Confirmed

ESTRADIOL; NORGESTIMATE

Brand Name : PREFEST

Dosage Form : TABLET;ORAL

Dosage Strength : 1MG,1MG;N/A,0.09MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1999-10-22

Application Number : 21040

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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