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01 1AUROBINDO PHARMA

02 2AUROBINDO PHARMA LTD

03 3BARR

04 1BARR LABS INC

05 2GLENMARK PHARMS LTD

06 1GLENMARK SPECLT

07 5JANSSEN PHARMS

08 2LUPIN LTD

09 1LUPIN PHARMS

10 1MYLAN

11 5NAARI PTE

12 1NOVAST LABS

13 2NOVAST LABS LTD

14 2ORTHO MCNEIL PHARM

15 2PH HEALTH

16 1TEVA WOMENS

17 3WATSON LABS

18 5XIROMED

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PharmaCompass

01

AIChE Annual Meeting
Not Confirmed
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AIChE Annual Meeting
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

AIChE Annual Meeting
Not Confirmed
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AIChE Annual Meeting
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

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Dosage Strength : 0.035MG;0.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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

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Dosage Strength : 0.035MG;0.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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

AIChE Annual Meeting
Not Confirmed
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AIChE Annual Meeting
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

AIChE Annual Meeting
Not Confirmed
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AIChE Annual Meeting
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

AIChE Annual Meeting
Not Confirmed
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AIChE Annual Meeting
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

AIChE Annual Meeting
Not Confirmed
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AIChE Annual Meeting
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

AIChE Annual Meeting
Not Confirmed
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AIChE Annual Meeting
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

AIChE Annual Meeting
Not Confirmed
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AIChE Annual Meeting
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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