Details for New Drug Application (NDA): 209741
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The generic ingredient in NEBIVOLOL HYDROCHLORIDE is nebivolol hydrochloride. There are fourteen drug master file entries for this compound. Nineteen suppliers are listed for this compound. Additional details are available on the nebivolol hydrochloride profile page.
Summary for 209741
Tradename: | NEBIVOLOL HYDROCHLORIDE |
Applicant: | Apotex |
Ingredient: | nebivolol hydrochloride |
Patents: | 0 |
Medical Subject Heading (MeSH) Categories for 209741
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | EQ 10MG BASE | ||||
Approval Date: | Feb 27, 2024 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | EQ 20MG BASE | ||||
Approval Date: | Feb 27, 2024 | TE: | AB | RLD: | No |
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