NDC 71610-477

VARDENAFIL

Vardenafil

VARDENAFIL is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Aphena Pharma Solutions - Tennessee, Llc. The primary component is Vardenafil Hydrochloride Trihydrate.

Product ID71610-477_9d2796f2-b596-4588-96c8-f99407d3e671
NDC71610-477
Product TypeHuman Prescription Drug
Proprietary NameVARDENAFIL
Generic NameVardenafil
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2018-11-01
Marketing CategoryANDA / ANDA
Application NumberANDA208960
Labeler NameAphena Pharma Solutions - Tennessee, LLC
Substance NameVARDENAFIL HYDROCHLORIDE TRIHYDRATE
Active Ingredient Strength20 mg/1
Pharm ClassesPhosphodiesterase 5 Inhibitor [EPC],Phosphodiesterase 5 Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 71610-477-02

2 TABLET, FILM COATED in 1 BOTTLE (71610-477-02)
Marketing Start Date2020-11-05
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "VARDENAFIL" or generic name "Vardenafil"

NDCBrand NameGeneric Name
33342-203VardenafilVardenafil
46708-235VardenafilVardenafil
51407-174VARDENAFILVARDENAFIL
62332-235VardenafilVardenafil
70710-1068VARDENAFILVARDENAFIL
70710-1069VARDENAFILVARDENAFIL
70710-1070VARDENAFILVARDENAFIL
70710-1071VARDENAFILVARDENAFIL
70771-1047VARDENAFILVARDENAFIL
70771-1048VARDENAFILVARDENAFIL
70771-1049VARDENAFILVARDENAFIL
70771-1050VARDENAFILVARDENAFIL
71610-477VARDENAFILVARDENAFIL
71610-643VARDENAFILVARDENAFIL

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