01 6UCB INC
01 6FILM, EXTENDED RELEASE;TRANSDERMAL
01 6RX
01 6NEUPRO
01 6Yes
RLD : Yes
TE Code :
Brand Name : NEUPRO
Dosage Form : FILM, EXTENDED RELEASE;TRANSDERMAL
Dosage Strength : 2MG/24HR
Approval Date : 2007-05-09
Application Number : 21829
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : NEUPRO
Dosage Form : FILM, EXTENDED RELEASE;TRANSDERMAL
Dosage Strength : 4MG/24HR
Approval Date : 2007-05-09
Application Number : 21829
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : NEUPRO
Dosage Form : FILM, EXTENDED RELEASE;TRANSDERMAL
Dosage Strength : 6MG/24HR
Approval Date : 2007-05-09
Application Number : 21829
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : NEUPRO
Dosage Form : FILM, EXTENDED RELEASE;TRANSDERMAL
Dosage Strength : 1MG/24HR
Approval Date : 2012-04-02
Application Number : 21829
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : NEUPRO
Dosage Form : FILM, EXTENDED RELEASE;TRANSDERMAL
Dosage Strength : 3MG/24HR
Approval Date : 2012-04-02
Application Number : 21829
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : NEUPRO
Dosage Form : FILM, EXTENDED RELEASE;TRANSDERMAL
Dosage Strength : 8MG/24HR
Approval Date : 2012-04-02
Application Number : 21829
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
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