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Approved Drug Products containing 208191 listed in the FDA Orange Book. Original Data : FDA Website

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01 DR REDDYS (3)

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01 TABLET;SUBLINGUAL (3)

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01 RX (3)

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01 NITROGLYCERIN (3)

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01 No (3)

URL Supplier Web Content
TABLET; SUBLINGUAL
0.3MG
2016-08-26
208191
NITROGLYCERIN
RX
No
AB
URL Supplier Web Content
TABLET; SUBLINGUAL
0.4MG
2016-08-26
208191
NITROGLYCERIN
RX
No
AB
URL Supplier Web Content
TABLET; SUBLINGUAL
0.6MG
2016-08-26
208191
NITROGLYCERIN
RX
No
AB

Looking for FDA Orange Book APPLICATION 208191

Looking for FDA Orange Book APPLICATION 208191 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 NITROGLYCERIN, with a corresponding application number 208191.

Regulatory Information RX

With a dosage strength 0.3MG

Dosage Form Route TABLET; SUBLINGUAL

Reference Listed Drug No

Approved since 2016-08-26

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 NITROGLYCERIN, with a corresponding application number 208191.

Regulatory Information RX

With a dosage strength 0.4MG

Dosage Form Route TABLET; SUBLINGUAL

Reference Listed Drug No

Approved since 2016-08-26

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 NITROGLYCERIN, with a corresponding application number 208191.

Regulatory Information RX

With a dosage strength 0.6MG

Dosage Form Route TABLET; SUBLINGUAL

Reference Listed Drug No

Approved since 2016-08-26

Therapeutic Equivalence (TE) Code AB

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