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PharmaCompass

01

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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CUPRIC SULFATE; MANGANESE SULFATE; SELENIOUS ACID; ZINC SULFATE

Brand Name : TRALEMENT

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : EQ 0.3MG COPPER/ML;EQ 55MCG BASE/ML;EQ 60MCG SELENIUM/ML;EQ 3MG BASE/ML (1ML)

Approval Date : 2020-07-02

Application Number : 209376

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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02

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CUPRIC SULFATE; MANGANESE SULFATE; SELENIOUS ACID; ZINC SULFATE

Brand Name : TRALEMENT

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : EQ 0.3MG COPPER/ML;EQ 55MCG BASE/ML;EQ 60MCG SELENIUM/ML;EQ 3MG BASE/ML (5ML)

Approval Date : 2020-12-02

Application Number : 209376

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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03

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CUPRIC SULFATE; MANGANESE SULFATE; SELENIOUS ACID; ZINC SULFATE

Brand Name : MULTRYS

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : EQ 60MCG COPPER/ML;EQ 3MCG BASE/ML;EQ 6MCG SELENIUM/ML;EQ 1000MCG BASE/ML (1ML)

Approval Date : 2021-06-30

Application Number : 209376

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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04

Pharmtech & Ingredients
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Pharmtech & Ingredients
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SELENIOUS ACID

Brand Name : SELENIOUS ACID

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : EQ 600MCG SELENIUM/10ML (EQ 60MCG SELENIUM/ML)

Approval Date : 2019-04-30

Application Number : 209379

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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05

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

SELENIOUS ACID

Brand Name : SELENIOUS ACID

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : EQ 60MCG SELENIUM/ML (EQ 60MCG SELENIUM/ML)

Approval Date : 2021-01-25

Application Number : 209379

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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06

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

SELENIOUS ACID

Brand Name : SELENIOUS ACID

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : EQ 12MCG SELENIUM/2ML (EQ 6MCG SELENIUM/ML)

Approval Date : 2021-08-30

Application Number : 209379

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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