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Approved Drug Products containing 202971 listed in the FDA Orange Book. Original Data : FDA Website

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01 OTSUKA PHARM CO LTD (4)

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01 FOR SUSPENSION, EXTENDED RELEASE;INTRAMUSCULAR (4)

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01 RX (4)

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01 ABILIFY MAINTENA KIT (4)

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01 Yes (4)

URL Supplier Web Content
FOR SUSPENSION, EX...
400MG
2014-09-29
202971
ABILIFY MAINTENA K...
RX
Yes
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URL Supplier Web Content
FOR SUSPENSION, EX...
400MG/VIAL
2013-02-28
202971
ABILIFY MAINTENA K...
RX
Yes
ASK
US
PHARMACOMPASS
Upload
your Marketing & Sales content
URL Supplier Web Content
FOR SUSPENSION, EX...
300MG
2014-09-29
202971
ABILIFY MAINTENA K...
RX
Yes
ASK
US
PHARMACOMPASS
Upload
your Marketing & Sales content
URL Supplier Web Content
FOR SUSPENSION, EX...
300MG/VIAL
2013-02-28
202971
ABILIFY MAINTENA K...
RX
Yes
ASK
US
PHARMACOMPASS
Upload
your Marketing & Sales content

Looking for FDA Orange Book APPLICATION 202971

Looking for FDA Orange Book APPLICATION 202971 4

19

Opocrin SpA, based in Italy, is a pharmaceutical company.

One of their notable products is ARIPIPRAZOLE, with a corresponding application number 202971.

Regulatory Information RX

With a dosage strength 400MG

Dosage Form Route FOR SUSPENSION, EXTENDED RELEASE; INTRAMUSCULAR

Reference Listed Drug Yes

Approved since 2014-09-29

18

Opocrin SpA, based in Italy, is a pharmaceutical company.

One of their notable products is ARIPIPRAZOLE, with a corresponding application number 202971.

Regulatory Information RX

With a dosage strength 400MG/VIAL

Dosage Form Route FOR SUSPENSION, EXTENDED RELEASE; INTRAMUSCULAR

Reference Listed Drug Yes

Approved since 2013-02-28

17

Opocrin SpA, based in Italy, is a pharmaceutical company.

One of their notable products is ARIPIPRAZOLE, with a corresponding application number 202971.

Regulatory Information RX

With a dosage strength 300MG

Dosage Form Route FOR SUSPENSION, EXTENDED RELEASE; INTRAMUSCULAR

Reference Listed Drug Yes

Approved since 2014-09-29

16

Opocrin SpA, based in Italy, is a pharmaceutical company.

One of their notable products is ARIPIPRAZOLE, with a corresponding application number 202971.

Regulatory Information RX

With a dosage strength 300MG/VIAL

Dosage Form Route FOR SUSPENSION, EXTENDED RELEASE; INTRAMUSCULAR

Reference Listed Drug Yes

Approved since 2013-02-28

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