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FDA ANDA · ANDA206729

NEBIVOLOL HYDROCHLORIDE

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APPLICATION
ANDA206729
TYPE
ANDA
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
None (Tentative Approval)

Products

NEBIVOLOL HYDROCHLORIDENone (Tentative Approval)
NEBIVOLOL HYDROCHLORIDE 10MG · TABLET · ORAL
NEBIVOLOL HYDROCHLORIDENone (Tentative Approval)
NEBIVOLOL HYDROCHLORIDE 2.5MG · TABLET · ORAL
NEBIVOLOL HYDROCHLORIDENone (Tentative Approval)
NEBIVOLOL HYDROCHLORIDE 20MG · TABLET · ORAL
NEBIVOLOL HYDROCHLORIDENone (Tentative Approval)
NEBIVOLOL HYDROCHLORIDE 5MG · TABLET · ORAL

Approval history

2020-12-28UNKNOWN · Original · standardTA
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Source: FDA Drugs@FDA. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data, not medical, legal, or regulatory advice.

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