NDC 68462-618

nebivolol

Nebivolol Hydrochloride

nebivolol is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Glenmark Pharmaceuticals Inc., Usa. The primary component is Nebivolol Hydrochloride.

Product ID68462-618_cb47560d-9e35-4b0f-b12b-6ea478684a5b
NDC68462-618
Product TypeHuman Prescription Drug
Proprietary Namenebivolol
Generic NameNebivolol Hydrochloride
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2017-05-25
Marketing CategoryANDA /
Application NumberANDA203821
Labeler NameGlenmark Pharmaceuticals Inc., USA
Substance NameNEBIVOLOL HYDROCHLORIDE
Active Ingredient Strength20 mg/1
Pharm ClassesAdrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 68462-618-01

100 TABLET in 1 BOTTLE (68462-618-01)
Marketing Start Date2017-05-25
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "nebivolol" or generic name "Nebivolol Hydrochloride"

NDCBrand NameGeneric Name
0904-7189nebivololnebivolol
0904-7190nebivololnebivolol
0904-7225nebivololnebivolol
0904-7226nebivololnebivolol
13668-353nebivololnebivolol
13668-354nebivololnebivolol
43975-248NebivololNebivolol
43975-250NebivololNebivolol
43975-249NebivololNebivolol
43975-251NebivololNebivolol
0456-1402Bystolicnebivolol hydrochloride
0456-1405Bystolicnebivolol hydrochloride
0456-1410Bystolicnebivolol hydrochloride
0456-1420Bystolicnebivolol hydrochloride

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