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Approved Drug Products containing 77751 listed in the FDA Orange Book. Original Data : FDA Website

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01 ZYDUS PHARMS USA (4)

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01 TABLET;ORAL (4)

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01 DISCN (1)

02 RX (3)

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01 PRAVASTATIN SODIUM (4)

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01 No (4)

URL Supplier Web Content
TABLET; ORAL
80MG
2008-04-30
77751
PRAVASTATIN SODIUM
RX
No
AB
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URL Supplier Web Content
TABLET; ORAL
20MG
2008-04-30
77751
PRAVASTATIN SODIUM
RX
No
AB
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URL Supplier Web Content
TABLET; ORAL
40MG
2008-04-30
77751
PRAVASTATIN SODIUM
RX
No
AB
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PHARMACOMPASS
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URL Supplier Web Content
TABLET; ORAL
10MG
2008-04-30
77751
PRAVASTATIN SODIUM
DISCN
No
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US
PHARMACOMPASS
Upload
your Marketing & Sales content

Looking for FDA Orange Book APPLICATION 77751

Looking for FDA Orange Book APPLICATION 77751 4

19

Zydus Pharmaceuticals, based in U.S.A, is a pharmaceutical company.

One of their notable products is PRAVASTATIN SODIUM, with a corresponding application number 77751.

Regulatory Information RX

With a dosage strength 80MG

Dosage Form Route TABLET; ORAL

Reference Listed Drug No

Approved since 2008-04-30

Therapeutic Equivalence (TE) Code AB

18

Zydus Pharmaceuticals, based in U.S.A, is a pharmaceutical company.

One of their notable products is PRAVASTATIN SODIUM, with a corresponding application number 77751.

Regulatory Information RX

With a dosage strength 20MG

Dosage Form Route TABLET; ORAL

Reference Listed Drug No

Approved since 2008-04-30

Therapeutic Equivalence (TE) Code AB

17

Zydus Pharmaceuticals, based in U.S.A, is a pharmaceutical company.

One of their notable products is PRAVASTATIN SODIUM, with a corresponding application number 77751.

Regulatory Information RX

With a dosage strength 40MG

Dosage Form Route TABLET; ORAL

Reference Listed Drug No

Approved since 2008-04-30

Therapeutic Equivalence (TE) Code AB

16

Zydus Pharmaceuticals, based in U.S.A, is a pharmaceutical company.

One of their notable products is PRAVASTATIN SODIUM, with a corresponding application number 77751.

Regulatory Information DISCN

With a dosage strength 10MG

Dosage Form Route TABLET; ORAL

Reference Listed Drug No

Approved since 2008-04-30

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