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. Twenty-five 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: | DISCN | Dosage: | TABLET;ORAL | Strength | EQ 10MG BASE | ||||
| Approval Date: | Feb 27, 2024 | TE: | RLD: | No | |||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | EQ 20MG BASE | ||||
| Approval Date: | Feb 27, 2024 | TE: | RLD: | No | |||||
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