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Approved Drug Products containing 76710 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 LEVOFLOXACIN (3)

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01 No (3)

URL Supplier Web Content
TABLET; ORAL
750MG
2011-06-20
76710
LEVOFLOXACIN
RX
No
AB
URL Supplier Web Content
TABLET; ORAL
250MG
2011-06-20
76710
LEVOFLOXACIN
RX
No
AB
URL Supplier Web Content
TABLET; ORAL
500MG
2011-06-20
76710
LEVOFLOXACIN
RX
No
AB

Looking for FDA Orange Book APPLICATION 76710

Looking for FDA Orange Book APPLICATION 76710 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 LEVOFLOXACIN, with a corresponding application number 76710.

Regulatory Information RX

With a dosage strength 750MG

Dosage Form Route TABLET; ORAL

Reference Listed Drug No

Approved since 2011-06-20

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 LEVOFLOXACIN, with a corresponding application number 76710.

Regulatory Information RX

With a dosage strength 250MG

Dosage Form Route TABLET; ORAL

Reference Listed Drug No

Approved since 2011-06-20

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 LEVOFLOXACIN, with a corresponding application number 76710.

Regulatory Information RX

With a dosage strength 500MG

Dosage Form Route TABLET; ORAL

Reference Listed Drug No

Approved since 2011-06-20

Therapeutic Equivalence (TE) Code AB

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