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Approved Drug Products containing 21434 listed in the FDA Orange Book. Original Data : FDA Website

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01 UPJOHN (4)

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01 TABLET, EXTENDED RELEASE;ORAL (4)

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01 RX (4)

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01 XANAX XR (4)

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01 Yes (4)

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TABLET, EXTENDED R...
0.5MG
2003-01-17
21434
XANAX XR
RX
Yes
AB
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TABLET, EXTENDED R...
3MG
2003-01-17
21434
XANAX XR
RX
Yes
AB
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TABLET, EXTENDED R...
1MG
2003-01-17
21434
XANAX XR
RX
Yes
AB
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TABLET, EXTENDED R...
2MG
2003-01-17
21434
XANAX XR
RX
Yes
AB
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Looking for FDA Orange Book APPLICATION 21434

Looking for FDA Orange Book APPLICATION 21434 4

19

Pfizer Inc, based in U.S.A, is a pharmaceutical company that stands out with its certifications from FDA, EDQM and WHO-GMP.

One of their notable products is ALPRAZOLAM, with a corresponding application number 21434.

Regulatory Information RX

With a dosage strength 0.5MG

Dosage Form Route TABLET, EXTENDED RELEASE; ORAL

Reference Listed Drug Yes

Approved since 2003-01-17

Therapeutic Equivalence (TE) Code AB

18

Pfizer Inc, based in U.S.A, is a pharmaceutical company that stands out with its certifications from FDA, EDQM and WHO-GMP.

One of their notable products is ALPRAZOLAM, with a corresponding application number 21434.

Regulatory Information RX

With a dosage strength 3MG

Dosage Form Route TABLET, EXTENDED RELEASE; ORAL

Reference Listed Drug Yes

Approved since 2003-01-17

Therapeutic Equivalence (TE) Code AB

17

Pfizer Inc, based in U.S.A, is a pharmaceutical company that stands out with its certifications from FDA, EDQM and WHO-GMP.

One of their notable products is ALPRAZOLAM, with a corresponding application number 21434.

Regulatory Information RX

With a dosage strength 1MG

Dosage Form Route TABLET, EXTENDED RELEASE; ORAL

Reference Listed Drug Yes

Approved since 2003-01-17

Therapeutic Equivalence (TE) Code AB

16

Pfizer Inc, based in U.S.A, is a pharmaceutical company that stands out with its certifications from FDA, EDQM and WHO-GMP.

One of their notable products is ALPRAZOLAM, with a corresponding application number 21434.

Regulatory Information RX

With a dosage strength 2MG

Dosage Form Route TABLET, EXTENDED RELEASE; ORAL

Reference Listed Drug Yes

Approved since 2003-01-17

Therapeutic Equivalence (TE) Code AB

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