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Approved Drug Products containing 74890 listed in the FDA Orange Book. Original Data : FDA Website

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01 HIKMA (4)

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01 TABLET;ORAL (4)

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01 DISCN (4)

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01 CIMETIDINE (4)

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01 No (4)

URL Supplier Web Content
TABLET; ORAL
800MG
1998-12-18
74890
CIMETIDINE
DISCN
No
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URL Supplier Web Content
TABLET; ORAL
300MG
1998-12-18
74890
CIMETIDINE
DISCN
No
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URL Supplier Web Content
TABLET; ORAL
400MG
1998-12-18
74890
CIMETIDINE
DISCN
No
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URL Supplier Web Content
TABLET; ORAL
200MG
1998-12-18
74890
CIMETIDINE
DISCN
No
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Looking for FDA Orange Book APPLICATION 74890

Looking for FDA Orange Book APPLICATION 74890 4

19

Hikma Pharmaceuticals, based in United Kingdom, is a pharmaceutical company that stands out with its certifications from FDA and EDQM.

One of their notable products is CIMETIDINE, with a corresponding application number 74890.

Regulatory Information DISCN

With a dosage strength 800MG

Dosage Form Route TABLET; ORAL

Reference Listed Drug No

Approved since 1998-12-18

18

Hikma Pharmaceuticals, based in United Kingdom, is a pharmaceutical company that stands out with its certifications from FDA and EDQM.

One of their notable products is CIMETIDINE, with a corresponding application number 74890.

Regulatory Information DISCN

With a dosage strength 300MG

Dosage Form Route TABLET; ORAL

Reference Listed Drug No

Approved since 1998-12-18

17

Hikma Pharmaceuticals, based in United Kingdom, is a pharmaceutical company that stands out with its certifications from FDA and EDQM.

One of their notable products is CIMETIDINE, with a corresponding application number 74890.

Regulatory Information DISCN

With a dosage strength 400MG

Dosage Form Route TABLET; ORAL

Reference Listed Drug No

Approved since 1998-12-18

16

Hikma Pharmaceuticals, based in United Kingdom, is a pharmaceutical company that stands out with its certifications from FDA and EDQM.

One of their notable products is CIMETIDINE, with a corresponding application number 74890.

Regulatory Information DISCN

With a dosage strength 200MG

Dosage Form Route TABLET; ORAL

Reference Listed Drug No

Approved since 1998-12-18

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