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Approved Drug Products containing 76649 listed in the FDA Orange Book. Original Data : FDA Website

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01 DR REDDYS LABS LTD (4)

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01 TABLET;ORAL (4)

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01 RX (4)

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01 CARVEDILOL (4)

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01 No (4)

URL Supplier Web Content
TABLET; ORAL
25MG
2007-09-05
76649
CARVEDILOL
RX
No
AB
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URL Supplier Web Content
TABLET; ORAL
6.25MG
2007-09-05
76649
CARVEDILOL
RX
No
AB
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URL Supplier Web Content
TABLET; ORAL
12.5MG
2007-09-05
76649
CARVEDILOL
RX
No
AB
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TABLET; ORAL
3.125MG
2007-09-05
76649
CARVEDILOL
RX
No
AB
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Looking for FDA Orange Book APPLICATION 76649

Looking for FDA Orange Book APPLICATION 76649 4

19

XYZ Pharma, based in Gabon, is a pharmaceutical company that stands out with its certifications from FDA and EDQM.

One of their notable products is CARVEDILOL, with a corresponding application number 76649.

Regulatory Information RX

With a dosage strength 25MG

Dosage Form Route TABLET; ORAL

Reference Listed Drug No

Approved since 2007-09-05

Therapeutic Equivalence (TE) Code AB

18

XYZ Pharma, based in Gabon, is a pharmaceutical company that stands out with its certifications from FDA and EDQM.

One of their notable products is CARVEDILOL, with a corresponding application number 76649.

Regulatory Information RX

With a dosage strength 6.25MG

Dosage Form Route TABLET; ORAL

Reference Listed Drug No

Approved since 2007-09-05

Therapeutic Equivalence (TE) Code AB

17

XYZ Pharma, based in Gabon, is a pharmaceutical company that stands out with its certifications from FDA and EDQM.

One of their notable products is CARVEDILOL, with a corresponding application number 76649.

Regulatory Information RX

With a dosage strength 12.5MG

Dosage Form Route TABLET; ORAL

Reference Listed Drug No

Approved since 2007-09-05

Therapeutic Equivalence (TE) Code AB

16

XYZ Pharma, based in Gabon, is a pharmaceutical company that stands out with its certifications from FDA and EDQM.

One of their notable products is CARVEDILOL, with a corresponding application number 76649.

Regulatory Information RX

With a dosage strength 3.125MG

Dosage Form Route TABLET; ORAL

Reference Listed Drug No

Approved since 2007-09-05

Therapeutic Equivalence (TE) Code AB

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