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01 3AMINOCAPROIC ACID

02 2ETRAVIRINE

03 1FAMOTIDINE

04 2PRIMIDONE

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PharmaCompass

01

Brand Name : AMINOCAPROIC ACID

Pharmtech & Ingredients
Not Confirmed
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Brand Name : AMINOCAPROIC ACID

Pharmtech & Ingredients
Not Confirmed
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Carnegie Pharmaceuticals

Dosage Form : TABLET; ORAL

Proprietary Name : AMINOCAPROIC ACID

Dosage Strength : 500MG

Approval Date : 2021-02-12

Application Number : 213928

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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02

Brand Name : AMINOCAPROIC ACID

Pharmtech & Ingredients
Not Confirmed
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Brand Name : AMINOCAPROIC ACID

Pharmtech & Ingredients
Not Confirmed
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Carnegie Pharmaceuticals

Dosage Form : TABLET; ORAL

Proprietary Name : AMINOCAPROIC ACID

Dosage Strength : 1GM

Approval Date : 2021-02-12

Application Number : 213928

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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03

Brand Name : AMINOCAPROIC ACID

Fi Europe 2024
Not Confirmed
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Brand Name : AMINOCAPROIC ACID

Fi Europe 2024
Not Confirmed
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Carnegie Pharmaceuticals

Dosage Form : SOLUTION; ORAL

Proprietary Name : AMINOCAPROIC ACID

Dosage Strength : 0.25GM/ML

Approval Date : 2021-01-26

Application Number : 214140

RX/OTC/DISCN : RX

RLD : No

TE Code : AA

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04

Brand Name : ETRAVIRINE

Pharmtech & Ingredients
Not Confirmed
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Brand Name : ETRAVIRINE

Pharmtech & Ingredients
Not Confirmed
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Carnegie Pharmaceuticals

Dosage Form : TABLET; ORAL

Proprietary Name : ETRAVIRINE

Dosage Strength : 100MG

Approval Date : 2022-04-13

Application Number : 215402

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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05

Brand Name : ETRAVIRINE

Pharmtech & Ingredients
Not Confirmed
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Brand Name : ETRAVIRINE

Pharmtech & Ingredients
Not Confirmed
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Carnegie Pharmaceuticals

Dosage Form : TABLET; ORAL

Proprietary Name : ETRAVIRINE

Dosage Strength : 200MG

Approval Date : 2022-04-13

Application Number : 215402

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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06

Brand Name : FAMOTIDINE

Pharmtech & Ingredients
Not Confirmed
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Brand Name : FAMOTIDINE

Pharmtech & Ingredients
Not Confirmed
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Carnegie Pharmaceuticals

Dosage Form : FOR SUSPENSION; ORAL

Proprietary Name : FAMOTIDINE

Dosage Strength : 40MG/5ML

Approval Date : 2023-07-07

Application Number : 217137

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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07

Brand Name : PRIMIDONE

Pharmtech & Ingredients
Not Confirmed
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Brand Name : PRIMIDONE

Pharmtech & Ingredients
Not Confirmed
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Carnegie Pharmaceuticals

Dosage Form : TABLET; ORAL

Proprietary Name : PRIMIDONE

Dosage Strength : 50MG

Approval Date : 2024-01-23

Application Number : 218366

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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08

Brand Name : PRIMIDONE

Pharmtech & Ingredients
Not Confirmed
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Brand Name : PRIMIDONE

Pharmtech & Ingredients
Not Confirmed
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Carnegie Pharmaceuticals

Dosage Form : TABLET; ORAL

Proprietary Name : PRIMIDONE

Dosage Strength : 250MG

Approval Date : 2024-01-23

Application Number : 218366

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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