Bystolic
- Product NDC
- 50090-3326
- 11-digit product format
- 500903326
- Labeler code
- 50090
- Product ID
- 50090-3326_6fe56b32-71ad-4a09-996c-0fb376b006cd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- nebivolol hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- NDA021742
- Marketing category
- NDA
- Marketing start
- 2008-01-22
- Marketing end
- 0000-00-00
- Substance
- NEBIVOLOL HYDROCHLORIDE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-3326-0 | 50090332600 | 30 TABLET in 1 BOTTLE (50090-3326-0) | 30 tablet | 2018-01-09 | 0000-00-00 | No | No | Current |