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Approved Drug Products containing 201722 listed in the FDA Orange Book. Original Data : FDA Website

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01 SUN PHARM INDUSTRIES (3)

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01 CAPSULE;ORAL (3)

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01 RX (3)

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01 NITROFURANTOIN (3)

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01 No (3)

URL Supplier Web Content
CAPSULE; ORAL
50MG
2016-02-16
201722
NITROFURANTOIN
RX
No
AB
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URL Supplier Web Content
CAPSULE; ORAL
100MG
2016-02-16
201722
NITROFURANTOIN
RX
No
AB
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PHARMACOMPASS
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your Marketing & Sales content
URL Supplier Web Content
CAPSULE; ORAL
25MG
2016-02-16
201722
NITROFURANTOIN
RX
No
AB
ASK
US
PHARMACOMPASS
Upload
your Marketing & Sales content

Looking for FDA Orange Book APPLICATION 201722

Looking for FDA Orange Book APPLICATION 201722 3

19

Sun Pharmaceutical Industries 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 NITROFURANTOIN, MACROCRYSTALLINE, with a corresponding application number 201722.

Regulatory Information RX

With a dosage strength 50MG

Dosage Form Route CAPSULE; ORAL

Reference Listed Drug No

Approved since 2016-02-16

Therapeutic Equivalence (TE) Code AB

18

Sun Pharmaceutical Industries 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 NITROFURANTOIN, MACROCRYSTALLINE, with a corresponding application number 201722.

Regulatory Information RX

With a dosage strength 100MG

Dosage Form Route CAPSULE; ORAL

Reference Listed Drug No

Approved since 2016-02-16

Therapeutic Equivalence (TE) Code AB

17

Sun Pharmaceutical Industries 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 NITROFURANTOIN, MACROCRYSTALLINE, with a corresponding application number 201722.

Regulatory Information RX

With a dosage strength 25MG

Dosage Form Route CAPSULE; ORAL

Reference Listed Drug No

Approved since 2016-02-16

Therapeutic Equivalence (TE) Code AB

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