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Approved Drug Products containing 20987 listed in the FDA Orange Book. Original Data : FDA Website

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01 WYETH PHARMS (2)

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01 TABLET, DELAYED RELEASE;ORAL (2)

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01 RX (2)

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01 PROTONIX (2)

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01 Yes (2)

URL Supplier Web Content
TABLET, DELAYED RE...
EQ 20MG BASE
2001-06-12
20987
PROTONIX
RX
Yes
AB
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URL Supplier Web Content
TABLET, DELAYED RE...
EQ 40MG BASE
2000-02-02
20987
PROTONIX
RX
Yes
AB
ASK
US
PHARMACOMPASS
Upload
your Marketing & Sales content

Looking for FDA Orange Book APPLICATION 20987

Looking for FDA Orange Book APPLICATION 20987 2

19

Wyeth Pharmaceuticals Inc, based in U.S.A, is a pharmaceutical company that stands out with its certifications from FDA and EDQM.

One of their notable products is PANTOPRAZOLE SODIUM, with a corresponding application number 20987.

Regulatory Information RX

With a dosage strength EQ 20MG BASE

Dosage Form Route TABLET, DELAYED RELEASE; ORAL

Reference Listed Drug Yes

Approved since 2001-06-12

Therapeutic Equivalence (TE) Code AB

18

Wyeth Pharmaceuticals Inc, based in U.S.A, is a pharmaceutical company that stands out with its certifications from FDA and EDQM.

One of their notable products is PANTOPRAZOLE SODIUM, with a corresponding application number 20987.

Regulatory Information RX

With a dosage strength EQ 40MG BASE

Dosage Form Route TABLET, DELAYED RELEASE; ORAL

Reference Listed Drug Yes

Approved since 2000-02-02

Therapeutic Equivalence (TE) Code AB

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