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01 1ABRAXIS PHARM

02 4AM REGENT

03 1APOTEX CORP

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PharmaCompass

01

Antibody Engineering
Not Confirmed
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Antibody Engineering
Not Confirmed

CUPRIC SULFATE

Brand Name : CUPRIC SULFATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 0.4MG COPPER/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1987-05-05

Application Number : 19350

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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02

Antibody Engineering
Not Confirmed
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Antibody Engineering
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 (1ML)

Approval Date : 2020-07-02

Application Number : 209376

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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03

Antibody Engineering
Not Confirmed
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Antibody Engineering
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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04

Antibody Engineering
Not Confirmed
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Antibody Engineering
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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05

Antibody Engineering
Not Confirmed
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Antibody Engineering
Not Confirmed

CUPRIC SULFATE

Brand Name : CUPRIC SULFATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 0.4MG COPPER/ML

Approval Date : 2022-12-16

Application Number : 216324

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

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06

Antibody Engineering
Not Confirmed
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Antibody Engineering
Not Confirmed

CUPRIC SULFATE

Brand Name : CUPRIC SULFATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 0.4MG COPPER/ML

Approval Date : 2024-08-19

Application Number : 218745

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

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