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01 3ABBVIE

02 1APOTEX INC

03 1BAUSCH AND LOMB

04 1NOVARTIS

05 1SANDOZ

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PharmaCompass

01

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CPhI India 2024
Not Confirmed

CARTEOLOL HYDROCHLORIDE

Brand Name : CARTROL

Dosage Form : TABLET;ORAL

Dosage Strength : 2.5MG

Approval Date : 1988-12-28

Application Number : 19204

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Abbvie Company Banner

02

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CPhI India 2024
Not Confirmed

CARTEOLOL HYDROCHLORIDE

Brand Name : CARTROL

Dosage Form : TABLET;ORAL

Dosage Strength : 5MG

Approval Date : 1988-12-28

Application Number : 19204

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Abbvie Company Banner

03

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CPhI India 2024
Not Confirmed

CARTEOLOL HYDROCHLORIDE

Brand Name : CARTROL

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG

Approval Date : 1988-12-28

Application Number : 19204

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Abbvie Company Banner

04

CPhI India 2024
Not Confirmed
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CPhI India 2024
Not Confirmed

CARTEOLOL HYDROCHLORIDE

Brand Name : CARTEOLOL HYDROCHLORIDE

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : 1%

Approval Date : 2002-02-06

Application Number : 76097

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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05

CPhI India 2024
Not Confirmed
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CPhI India 2024
Not Confirmed

CARTEOLOL HYDROCHLORIDE

Brand Name : CARTEOLOL HYDROCHLORIDE

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : 1%

Approval Date : 2000-01-20

Application Number : 75546

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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06

CPhI India 2024
Not Confirmed
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CPhI India 2024
Not Confirmed

CARTEOLOL HYDROCHLORIDE

Brand Name : OCUPRESS

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : 1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1990-05-23

Application Number : 19972

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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07

CPhI India 2024
Not Confirmed
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CPhI India 2024
Not Confirmed

CARTEOLOL HYDROCHLORIDE

Brand Name : CARTEOLOL HYDROCHLORIDE

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : 1%

Approval Date : 2000-01-03

Application Number : 75476

RX/OTC/DISCN : RX

RLD : No

TE Code :

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