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Approved Drug Products containing 76262 listed in the FDA Orange Book. Original Data : FDA Website

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01 SANDOZ (3)

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01 TABLET;ORAL (3)

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01 RX (3)

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01 LISINOPRIL AND HYDROCHLOROTHIAZIDE (3)

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01 No (3)

URL Supplier Web Content
TABLET; ORAL
25MG;20MG
2002-07-01
76262
LISINOPRIL AND HYD...
RX
No
AB
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URL Supplier Web Content
TABLET; ORAL
12.5MG;10MG
2002-07-01
76262
LISINOPRIL AND HYD...
RX
No
AB
ASK
US
PHARMACOMPASS
Upload
your Marketing & Sales content
URL Supplier Web Content
TABLET; ORAL
12.5MG;20MG
2002-07-01
76262
LISINOPRIL AND HYD...
RX
No
AB
ASK
US
PHARMACOMPASS
Upload
your Marketing & Sales content

Looking for FDA Orange Book APPLICATION 76262

Looking for FDA Orange Book APPLICATION 76262 3

19

Sandoz B2B, based in Switzerland, is a pharmaceutical company that stands out with its certifications from FDA and EDQM.

They are recognized for A global leader in antibiotics.

One of their notable products is HYDROCHLOROTHIAZIDE; LISINOPRIL, with a corresponding application number 76262.

Regulatory Information RX

With a dosage strength 25MG;20MG

Dosage Form Route TABLET; ORAL

Reference Listed Drug No

Approved since 2002-07-01

Therapeutic Equivalence (TE) Code AB

18

Sandoz B2B, based in Switzerland, is a pharmaceutical company that stands out with its certifications from FDA and EDQM.

They are recognized for A global leader in antibiotics.

One of their notable products is HYDROCHLOROTHIAZIDE; LISINOPRIL, with a corresponding application number 76262.

Regulatory Information RX

With a dosage strength 12.5MG;10MG

Dosage Form Route TABLET; ORAL

Reference Listed Drug No

Approved since 2002-07-01

Therapeutic Equivalence (TE) Code AB

17

Sandoz B2B, based in Switzerland, is a pharmaceutical company that stands out with its certifications from FDA and EDQM.

They are recognized for A global leader in antibiotics.

One of their notable products is HYDROCHLOROTHIAZIDE; LISINOPRIL, with a corresponding application number 76262.

Regulatory Information RX

With a dosage strength 12.5MG;20MG

Dosage Form Route TABLET; ORAL

Reference Listed Drug No

Approved since 2002-07-01

Therapeutic Equivalence (TE) Code AB

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