NDC 67877-392

Nebivolol

Nebivolol

Nebivolol is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Ascend Laboratories, Llc. The primary component is Nebivolol Hydrochloride.

Product ID67877-392_0f1472cb-fa10-4ad1-b5c4-bee8798e8078
NDC67877-392
Product TypeHuman Prescription Drug
Proprietary NameNebivolol
Generic NameNebivolol
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2021-09-16
Marketing CategoryANDA /
Application NumberANDA203828
Labeler NameAscend Laboratories, LLC
Substance NameNEBIVOLOL HYDROCHLORIDE
Active Ingredient Strength5 mg/1
Pharm ClassesAdrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 67877-392-01

100 TABLET in 1 BOTTLE (67877-392-01)
Marketing Start Date2021-09-16
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

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