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01 5APOMORPHINE HYDROCHLORIDE

02 4ESLICARBAZEPINE ACETATE

03 1GLYCOPYRROLATE

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PharmaCompass

01

Brand Name : KYNMOBI

Pharmtech & Ingredients
Not Confirmed
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Brand Name : KYNMOBI

Pharmtech & Ingredients
Not Confirmed
arrow

Sumitomo Pharma America

Dosage Form : FILM; SUBLINGUAL

Proprietary Name : KYNMOBI

Dosage Strength : 10MG

Approval Date : 2020-05-21

Application Number : 210875

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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02

Brand Name : KYNMOBI

Pharmtech & Ingredients
Not Confirmed
arrow

Brand Name : KYNMOBI

Pharmtech & Ingredients
Not Confirmed
arrow

Sumitomo Pharma America

Dosage Form : FILM; SUBLINGUAL

Proprietary Name : KYNMOBI

Dosage Strength : 15MG

Approval Date : 2020-05-21

Application Number : 210875

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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03

Brand Name : KYNMOBI

Pharmtech & Ingredients
Not Confirmed
arrow

Brand Name : KYNMOBI

Pharmtech & Ingredients
Not Confirmed
arrow

Sumitomo Pharma America

Dosage Form : FILM; SUBLINGUAL

Proprietary Name : KYNMOBI

Dosage Strength : 20MG

Approval Date : 2020-05-21

Application Number : 210875

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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04

Brand Name : KYNMOBI

Pharmtech & Ingredients
Not Confirmed
arrow

Brand Name : KYNMOBI

Pharmtech & Ingredients
Not Confirmed
arrow

Sumitomo Pharma America

Dosage Form : FILM; SUBLINGUAL

Proprietary Name : KYNMOBI

Dosage Strength : 25MG

Approval Date : 2020-05-21

Application Number : 210875

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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05

Brand Name : KYNMOBI

Pharmtech & Ingredients
Not Confirmed
arrow

Brand Name : KYNMOBI

Pharmtech & Ingredients
Not Confirmed
arrow

Sumitomo Pharma America

Dosage Form : FILM; SUBLINGUAL

Proprietary Name : KYNMOBI

Dosage Strength : 30MG

Approval Date : 2020-05-21

Application Number : 210875

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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06

Brand Name : APTIOM

Pharmtech & Ingredients
Not Confirmed
arrow

Brand Name : APTIOM

Pharmtech & Ingredients
Not Confirmed
arrow

Sumitomo Pharma America

Dosage Form : TABLET; ORAL

Proprietary Name : APTIOM

Dosage Strength : 200MG

Approval Date : 2013-11-08

Application Number : 22416

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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07

Brand Name : APTIOM

Pharmtech & Ingredients
Not Confirmed
arrow

Brand Name : APTIOM

Pharmtech & Ingredients
Not Confirmed
arrow

Sumitomo Pharma America

Dosage Form : TABLET; ORAL

Proprietary Name : APTIOM

Dosage Strength : 400MG

Approval Date : 2013-11-08

Application Number : 22416

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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08

Brand Name : APTIOM

Pharmtech & Ingredients
Not Confirmed
arrow

Brand Name : APTIOM

Pharmtech & Ingredients
Not Confirmed
arrow

Sumitomo Pharma America

Dosage Form : TABLET; ORAL

Proprietary Name : APTIOM

Dosage Strength : 600MG

Approval Date : 2013-11-08

Application Number : 22416

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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09

Brand Name : APTIOM

Pharmtech & Ingredients
Not Confirmed
arrow

Brand Name : APTIOM

Pharmtech & Ingredients
Not Confirmed
arrow

Sumitomo Pharma America

Dosage Form : TABLET; ORAL

Proprietary Name : APTIOM

Dosage Strength : 800MG

Approval Date : 2013-11-08

Application Number : 22416

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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10

Brand Name : LONHALA MAGNAIR KIT

Pharmtech & Ingredients
Not Confirmed
arrow

Brand Name : LONHALA MAGNAIR KIT

Pharmtech & Ingredients
Not Confirmed
arrow

Sumitomo Pharma America

Dosage Form : SOLUTION; INHALATION

Proprietary Name : LONHALA MAGNAIR KIT

Dosage Strength : 25MCG/ML

Approval Date : 2017-12-05

Application Number : 208437

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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