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Approved Drug Products containing 208705 listed in the FDA Orange Book. Original Data : FDA Website

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01 ALEMBIC (2)

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01 CAPSULE, DELAYED RELEASE;ORAL (2)

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01 RX (2)

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01 FENOFIBRIC ACID (2)

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01 No (2)

URL Supplier Web Content
CAPSULE, DELAYED R...
EQ 135MG FENOFIBRI...
2017-05-12
208705
FENOFIBRIC ACID
RX
No
AB
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URL Supplier Web Content
CAPSULE, DELAYED R...
EQ 45MG FENOFIBRIC...
2017-05-12
208705
FENOFIBRIC ACID
RX
No
AB
ASK
US
PHARMACOMPASS
Upload
your Marketing & Sales content

Looking for FDA Orange Book APPLICATION 208705

Looking for FDA Orange Book APPLICATION 208705 2

19

Alembic Pharmaceuticals Limited, based in India, is a pharmaceutical company that stands out with its certifications from FDA, EDQM and WHO-GMP.

One of their notable products is CHOLINE FENOFIBRATE, with a corresponding application number 208705.

Regulatory Information RX

With a dosage strength EQ 135MG FENOFIBRIC ACID

Dosage Form Route CAPSULE, DELAYED RELEASE; ORAL

Reference Listed Drug No

Approved since 2017-05-12

Therapeutic Equivalence (TE) Code AB

18

Alembic Pharmaceuticals Limited, based in India, is a pharmaceutical company that stands out with its certifications from FDA, EDQM and WHO-GMP.

One of their notable products is CHOLINE FENOFIBRATE, with a corresponding application number 208705.

Regulatory Information RX

With a dosage strength EQ 45MG FENOFIBRIC ACID

Dosage Form Route CAPSULE, DELAYED RELEASE; ORAL

Reference Listed Drug No

Approved since 2017-05-12

Therapeutic Equivalence (TE) Code AB

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