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Approved Drug Products containing 76333 listed in the FDA Orange Book. Original Data : FDA Website

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01 ANI PHARMS (4)

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01 TABLET;ORAL (4)

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01 RX (4)

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01 BENAZEPRIL HYDROCHLORIDE (4)

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01 No (4)

URL Supplier Web Content
TABLET; ORAL
20MG
2004-02-11
76333
BENAZEPRIL HYDROCH...
RX
No
AB
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URL Supplier Web Content
TABLET; ORAL
5MG
2004-02-11
76333
BENAZEPRIL HYDROCH...
RX
No
AB
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URL Supplier Web Content
TABLET; ORAL
40MG
2004-02-11
76333
BENAZEPRIL HYDROCH...
RX
No
AB
ASK
US
PHARMACOMPASS
Upload
your Marketing & Sales content
URL Supplier Web Content
TABLET; ORAL
10MG
2004-02-11
76333
BENAZEPRIL HYDROCH...
RX
No
AB
ASK
US
PHARMACOMPASS
Upload
your Marketing & Sales content

Looking for FDA Orange Book APPLICATION 76333

Looking for FDA Orange Book APPLICATION 76333 4

19

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

One of their notable products is BENAZEPRIL HYDROCHLORIDE, with a corresponding application number 76333.

Regulatory Information RX

With a dosage strength 20MG

Dosage Form Route TABLET; ORAL

Reference Listed Drug No

Approved since 2004-02-11

Therapeutic Equivalence (TE) Code AB

18

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

One of their notable products is BENAZEPRIL HYDROCHLORIDE, with a corresponding application number 76333.

Regulatory Information RX

With a dosage strength 5MG

Dosage Form Route TABLET; ORAL

Reference Listed Drug No

Approved since 2004-02-11

Therapeutic Equivalence (TE) Code AB

17

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

One of their notable products is BENAZEPRIL HYDROCHLORIDE, with a corresponding application number 76333.

Regulatory Information RX

With a dosage strength 40MG

Dosage Form Route TABLET; ORAL

Reference Listed Drug No

Approved since 2004-02-11

Therapeutic Equivalence (TE) Code AB

16

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

One of their notable products is BENAZEPRIL HYDROCHLORIDE, with a corresponding application number 76333.

Regulatory Information RX

With a dosage strength 10MG

Dosage Form Route TABLET; ORAL

Reference Listed Drug No

Approved since 2004-02-11

Therapeutic Equivalence (TE) Code AB

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