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Approved Drug Products containing 203901 listed in the FDA Orange Book. Original Data : FDA Website

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01 ACTAVIS ELIZABETH (3)

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01 CAPSULE, EXTENDED RELEASE;ORAL (3)

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01 RX (3)

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01 DEXTROAMPHETAMINE SULFATE (3)

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01 No (3)

URL Supplier Web Content
CAPSULE, EXTENDED ...
15MG
2012-11-30
203901
DEXTROAMPHETAMINE ...
RX
No
AB
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URL Supplier Web Content
CAPSULE, EXTENDED ...
5MG
2012-11-30
203901
DEXTROAMPHETAMINE ...
RX
No
AB
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your Marketing & Sales content
URL Supplier Web Content
CAPSULE, EXTENDED ...
10MG
2012-11-30
203901
DEXTROAMPHETAMINE ...
RX
No
AB
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PHARMACOMPASS
Upload
your Marketing & Sales content

Looking for FDA Orange Book APPLICATION 203901

Looking for FDA Orange Book APPLICATION 203901 3

19

Actavis Inc, based in Ireland, is a pharmaceutical company that stands out with its certifications from FDA and EDQM.

One of their notable products is DEXTROAMPHETAMINE SULFATE, with a corresponding application number 203901.

Regulatory Information RX

With a dosage strength 15MG

Dosage Form Route CAPSULE, EXTENDED RELEASE; ORAL

Reference Listed Drug No

Approved since 2012-11-30

Therapeutic Equivalence (TE) Code AB

18

Actavis Inc, based in Ireland, is a pharmaceutical company that stands out with its certifications from FDA and EDQM.

One of their notable products is DEXTROAMPHETAMINE SULFATE, with a corresponding application number 203901.

Regulatory Information RX

With a dosage strength 5MG

Dosage Form Route CAPSULE, EXTENDED RELEASE; ORAL

Reference Listed Drug No

Approved since 2012-11-30

Therapeutic Equivalence (TE) Code AB

17

Actavis Inc, based in Ireland, is a pharmaceutical company that stands out with its certifications from FDA and EDQM.

One of their notable products is DEXTROAMPHETAMINE SULFATE, with a corresponding application number 203901.

Regulatory Information RX

With a dosage strength 10MG

Dosage Form Route CAPSULE, EXTENDED RELEASE; ORAL

Reference Listed Drug No

Approved since 2012-11-30

Therapeutic Equivalence (TE) Code AB

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