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01 1CIPROFLOXACIN HYDROCHLORIDE

02 1DORZOLAMIDE HYDROCHLORIDE

03 1DORZOLAMIDE HYDROCHLORIDE; TIMOLOL MALEATE

04 1LATANOPROST

05 2OFLOXACIN

06 1OLOPATADINE HYDROCHLORIDE

07 2TIMOLOL MALEATE

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PharmaCompass

01

Brand Name : CIPROFLOXACIN HYDROC...

Pharmtech & Ingredients
Not Confirmed
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Brand Name : CIPROFLOXACIN HYDROC...

Pharmtech & Ingredients
Not Confirmed
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FDC

Dosage Form : SOLUTION/DROPS; OPHTHALMIC

Proprietary Name : CIPROFLOXACIN HYDROCHLOR...

Dosage Strength : EQ 0.3% BASE

Approval Date : 2008-06-30

Application Number : 77568

RX/OTC/DISCN : RX

RLD : No

TE Code : AT

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02

Brand Name : DORZOLAMIDE HYDROCHL...

Pharmtech & Ingredients
Not Confirmed
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Brand Name : DORZOLAMIDE HYDROCHL...

Pharmtech & Ingredients
Not Confirmed
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FDC

Dosage Form : SOLUTION/DROPS; OPHTHALMIC

Proprietary Name : DORZOLAMIDE HYDROCHLORID...

Dosage Strength : EQ 2% BASE

Approval Date : 2019-01-24

Application Number : 205294

RX/OTC/DISCN : RX

RLD : No

TE Code : AT

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03

Brand Name : DORZOLAMIDE HYDROCHL...

Pharmtech & Ingredients
Not Confirmed
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Brand Name : DORZOLAMIDE HYDROCHL...

Pharmtech & Ingredients
Not Confirmed
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FDC

Dosage Form : SOLUTION/DROPS; OPHTHALMIC

Proprietary Name : DORZOLAMIDE HYDROCHLORID...

Dosage Strength : EQ 2% BASE;EQ 0.5% BASE

Approval Date : 2019-06-13

Application Number : 205295

RX/OTC/DISCN : RX

RLD : No

TE Code : AT1

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04

Brand Name : LATANOPROST

Pharmtech & Ingredients
Not Confirmed
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Brand Name : LATANOPROST

Pharmtech & Ingredients
Not Confirmed
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FDC

Dosage Form : SOLUTION/DROPS; OPHTHALMIC

Proprietary Name : LATANOPROST

Dosage Strength : 0.005%

Approval Date : 2016-04-22

Application Number : 202442

RX/OTC/DISCN : RX

RLD : No

TE Code : AT

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05

Brand Name : OFLOXACIN

Pharmtech & Ingredients
Not Confirmed
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Brand Name : OFLOXACIN

Pharmtech & Ingredients
Not Confirmed
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FDC

Dosage Form : SOLUTION/DROPS; OPHTHALMIC

Proprietary Name : OFLOXACIN

Dosage Strength : 0.3%

Approval Date : 2009-02-25

Application Number : 78559

RX/OTC/DISCN : RX

RLD : No

TE Code : AT

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06

Brand Name : OFLOXACIN

Pharmtech & Ingredients
Not Confirmed
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Brand Name : OFLOXACIN

Pharmtech & Ingredients
Not Confirmed
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FDC

Dosage Form : SOLUTION/DROPS; OTIC

Proprietary Name : OFLOXACIN

Dosage Strength : 0.3%

Approval Date : 2022-01-19

Application Number : 215038

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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07

Brand Name : OLOPATADINE HYDROCHL...

Pharmtech & Ingredients
Not Confirmed
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Brand Name : OLOPATADINE HYDROCHL...

Pharmtech & Ingredients
Not Confirmed
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FDC

Dosage Form : SOLUTION/DROPS; OPHTHALMIC

Proprietary Name : OLOPATADINE HYDROCHLORID...

Dosage Strength : EQ 0.1% BASE

Approval Date : 2019-09-26

Application Number : 209282

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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08

Brand Name : TIMOLOL MALEATE

Pharmtech & Ingredients
Not Confirmed
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Brand Name : TIMOLOL MALEATE

Pharmtech & Ingredients
Not Confirmed
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FDC

Dosage Form : SOLUTION/DROPS; OPHTHALMIC

Proprietary Name : TIMOLOL MALEATE

Dosage Strength : EQ 0.25% BASE

Approval Date : 2008-04-30

Application Number : 77259

RX/OTC/DISCN : RX

RLD : No

TE Code : AT1

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09

Brand Name : TIMOLOL MALEATE

Pharmtech & Ingredients
Not Confirmed
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Brand Name : TIMOLOL MALEATE

Pharmtech & Ingredients
Not Confirmed
arrow

FDC

Dosage Form : SOLUTION/DROPS; OPHTHALMIC

Proprietary Name : TIMOLOL MALEATE

Dosage Strength : EQ 0.5% BASE

Approval Date : 2008-04-30

Application Number : 77259

RX/OTC/DISCN : RX

RLD : No

TE Code : AT1

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Contact FDC and get a quotation

FDC is a supplier offers 30 products (APIs, Excipients or Intermediates).

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