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Approved Drug Products containing 21882 listed in the FDA Orange Book. Original Data : FDA Website

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01 NOVARTIS (3)

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01 TABLET, FOR SUSPENSION;ORAL (3)

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01 RX (3)

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01 EXJADE (3)

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01 Yes (3)

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TABLET, FOR SUSPEN...
500MG
2005-11-02
21882
EXJADE
RX
Yes
AB
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URL Supplier Web Content
TABLET, FOR SUSPEN...
125MG
2005-11-02
21882
EXJADE
RX
Yes
AB
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URL Supplier Web Content
TABLET, FOR SUSPEN...
250MG
2005-11-02
21882
EXJADE
RX
Yes
AB
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US
PHARMACOMPASS
Upload
your Marketing & Sales content

Looking for FDA Orange Book APPLICATION 21882

Looking for FDA Orange Book APPLICATION 21882 3

19

Novartis Pharmaceuticals Corporation, based in Switzerland, is a pharmaceutical company that stands out with its certifications from FDA, EDQM and WHO-GMP.

One of their notable products is DEFERASIROX, with a corresponding application number 21882.

Regulatory Information RX

With a dosage strength 500MG

Dosage Form Route TABLET, FOR SUSPENSION; ORAL

Reference Listed Drug Yes

Approved since 2005-11-02

Therapeutic Equivalence (TE) Code AB

18

Novartis Pharmaceuticals Corporation, based in Switzerland, is a pharmaceutical company that stands out with its certifications from FDA, EDQM and WHO-GMP.

One of their notable products is DEFERASIROX, with a corresponding application number 21882.

Regulatory Information RX

With a dosage strength 125MG

Dosage Form Route TABLET, FOR SUSPENSION; ORAL

Reference Listed Drug Yes

Approved since 2005-11-02

Therapeutic Equivalence (TE) Code AB

17

Novartis Pharmaceuticals Corporation, based in Switzerland, is a pharmaceutical company that stands out with its certifications from FDA, EDQM and WHO-GMP.

One of their notable products is DEFERASIROX, with a corresponding application number 21882.

Regulatory Information RX

With a dosage strength 250MG

Dosage Form Route TABLET, FOR SUSPENSION; ORAL

Reference Listed Drug Yes

Approved since 2005-11-02

Therapeutic Equivalence (TE) Code AB

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