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Suanfarma Suanfarma

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Approved Drug Products containing 76112 listed in the FDA Orange Book. Original Data : FDA Website

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01 DR REDDYS LABS INC (3)

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01 TABLET;ORAL (3)

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01 RX (3)

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01 IBUPROFEN (3)

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01 No (3)

URL Supplier Web Content
TABLET; ORAL
600MG
2001-10-31
76112
IBUPROFEN
RX
No
AB
URL Supplier Web Content
TABLET; ORAL
800MG
2001-10-31
76112
IBUPROFEN
RX
No
AB
URL Supplier Web Content
TABLET; ORAL
400MG
2001-10-31
76112
IBUPROFEN
RX
No
AB

Looking for FDA Orange Book APPLICATION 76112

Looking for FDA Orange Book APPLICATION 76112 3

19

Dr. Reddy\'s Laboratories, based in India, is a pharmaceutical company that stands out with its certifications from FDA and EDQM.

They are recognized for DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

One of their notable products is IBUPROFEN, with a corresponding application number 76112.

Regulatory Information RX

With a dosage strength 600MG

Dosage Form Route TABLET; ORAL

Reference Listed Drug No

Approved since 2001-10-31

Therapeutic Equivalence (TE) Code AB

18

Dr. Reddy\'s Laboratories, based in India, is a pharmaceutical company that stands out with its certifications from FDA and EDQM.

They are recognized for DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

One of their notable products is IBUPROFEN, with a corresponding application number 76112.

Regulatory Information RX

With a dosage strength 800MG

Dosage Form Route TABLET; ORAL

Reference Listed Drug No

Approved since 2001-10-31

Therapeutic Equivalence (TE) Code AB

17

Dr. Reddy\'s Laboratories, based in India, is a pharmaceutical company that stands out with its certifications from FDA and EDQM.

They are recognized for DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

One of their notable products is IBUPROFEN, with a corresponding application number 76112.

Regulatory Information RX

With a dosage strength 400MG

Dosage Form Route TABLET; ORAL

Reference Listed Drug No

Approved since 2001-10-31

Therapeutic Equivalence (TE) Code AB

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