01 1ABRAXIS PHARM
02 4AM REGENT
03 1APOTEX CORP
01 3INJECTABLE;INJECTION
02 3SOLUTION;INTRAVENOUS
01 1DISCN
02 5RX
01 3CUPRIC SULFATE
02 1MULTRYS
03 2TRALEMENT
01 2No
02 4Yes
RLD : Yes
TE Code :
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Dosage Strength : EQ 0.4MG COPPER/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 :
RLD : Yes
TE Code :
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 :
RLD : Yes
TE Code :
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 :
RLD : Yes
TE Code :
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 :
RLD : No
TE Code : AP
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
RLD : No
TE Code : AP
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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