Home
>
National Drug Code (NDC)
>
Bystolic
Bystolic - 55154-4621-8 - (nebivolol hydrochloride)
Drug Information of Bystolic
| Product NDC: | 55154-4621 |
| Proprietary Name: | Bystolic |
| Non Proprietary Name: | nebivolol hydrochloride |
| Active Ingredient(s): | 5 mg/1 & nbsp; nebivolol hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Bystolic
| Product NDC: | 55154-4621 |
| Labeler Name: | Cardinal Health |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021742 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20080122 |
Package Information of Bystolic
| Package NDC: | 55154-4621-8 |
| Package Description: | 3600 TABLET in 1 BOTTLE, PLASTIC (55154-4621-8) |
NDC Information of Bystolic
| NDC Code | 55154-4621-8 |
| Proprietary Name | Bystolic |
| Package Description | 3600 TABLET in 1 BOTTLE, PLASTIC (55154-4621-8) |
| Product NDC | 55154-4621 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | nebivolol hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20080122 |
| Marketing Category Name | NDA |
| Labeler Name | Cardinal Health |
| Substance Name | NEBIVOLOL HYDROCHLORIDE |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
