NDC 29300-375

Nebivolol Hydrochloride

Nebivolol Hydrochloride

Nebivolol Hydrochloride is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Unichem Pharmaceuticals (usa), Inc.. The primary component is Nebivolol Hydrochloride.

Product ID29300-375_a6807389-e7ea-4efa-a475-5db7038515e3
NDC29300-375
Product TypeHuman Prescription Drug
Proprietary NameNebivolol Hydrochloride
Generic NameNebivolol Hydrochloride
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2022-04-04
Marketing CategoryANDA /
Application NumberANDA213830
Labeler NameUnichem Pharmaceuticals (USA), Inc.
Substance NameNEBIVOLOL HYDROCHLORIDE
Active Ingredient Strength3 mg/1
Pharm ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 29300-375-05

500 TABLET in 1 BOTTLE (29300-375-05)
Marketing Start Date2022-04-04
NDC Exclude FlagN
Sample Package?N

Drug Details

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

NDCBrand NameGeneric Name
29300-375Nebivolol HydrochlorideNebivolol Hydrochloride
29300-376Nebivolol HydrochlorideNebivolol Hydrochloride
29300-377Nebivolol HydrochlorideNebivolol Hydrochloride
29300-378Nebivolol HydrochlorideNebivolol Hydrochloride
0456-1402Bystolicnebivolol hydrochloride
0456-1405Bystolicnebivolol hydrochloride
0456-1410Bystolicnebivolol hydrochloride
0456-1420Bystolicnebivolol hydrochloride
50090-1127Bystolicnebivolol hydrochloride
50090-1307Bystolicnebivolol hydrochloride
50090-3326Bystolicnebivolol hydrochloride
55154-4621Bystolicnebivolol hydrochloride
55154-4622Bystolicnebivolol hydrochloride
55154-4623Bystolicnebivolol hydrochloride

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