NDC 43547-525

NEBIVOLOL

Nebivolol

NEBIVOLOL is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Solco Healthcare Us, Llc. The primary component is Nebivolol.

Product ID43547-525_51d3f12f-94cc-4f58-94d3-61990e16adfc
NDC43547-525
Product TypeHuman Prescription Drug
Proprietary NameNEBIVOLOL
Generic NameNebivolol
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2022-02-14
Marketing CategoryANDA /
Application NumberANDA212682
Labeler NameSolco Healthcare US, LLC
Substance NameNEBIVOLOL
Active Ingredient Strength5 mg/1
Pharm ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 43547-525-03

30 TABLET in 1 BOTTLE (43547-525-03)
Marketing Start Date2022-02-14
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "NEBIVOLOL" or generic name "Nebivolol"

NDCBrand NameGeneric Name
0904-7189nebivololnebivolol
0904-7190nebivololnebivolol
0904-7225nebivololnebivolol
0904-7226nebivololnebivolol
13668-353nebivololnebivolol
13668-354nebivololnebivolol
13668-355nebivololnebivolol
13668-356nebivololnebivolol
43975-248NebivololNebivolol
43975-250NebivololNebivolol
43975-249NebivololNebivolol
43975-251NebivololNebivolol

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.