Byvalson
- Product NDC
- 0023-5874
- 11-digit product format
- 000235874
- Labeler code
- 0023
- Product ID
- 0023-5874_6964c0d8-8223-4992-b42c-43d3de03080e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- nebivolol hydrochloride and valsartan
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Allergan, Inc.
- Application
- NDA206302
- Marketing category
- NDA
- Marketing start
- 2016-06-03
- Marketing end
- 0000-00-00
- Substance
- NEBIVOLOL HYDROCHLORIDE; VALSARTAN
- Active strength
- 5 mg/1; mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC],Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record