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NDC 69238-1153-03 Vardenafil hydrochloride 20 mg/1 Details

Vardenafil hydrochloride 20 mg/1

Vardenafil hydrochloride is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Amneal Pharmaceuticals NY LLC. The primary component is VARDENAFIL HYDROCHLORIDE.

MedlinePlus Drug Summary

Vardenafil is used to treat erectile dysfunction (impotence; inability to get or keep an erection) in men. Vardenafil is in a class of medications called phosphodiesterase (PDE) inhibitors. It works by increasing blood flow to the penis during sexual stimulation. This increased blood flow can cause an erection. Vardenafil does not cure erectile dysfunction or increase sexual desire. Vardenafil does not prevent pregnancy or the spread of sexually transmitted diseases such as human immunodeficiency virus (HIV).

Related Packages: 69238-1153-03
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Vardenafil

Product Information

NDC	69238-1153
Product ID	69238-1153_12d047d4-2d50-4d2a-9f6b-22c13162b0c8
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Vardenafil hydrochloride
Proprietary Name Suffix	n/a
Non-Proprietary Name	Vardenafil hydrochloride
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, FILM COATED
Route	ORAL
Active Ingredient Strength	20
Active Ingredient Units	mg/1
Substance Name	VARDENAFIL HYDROCHLORIDE
Labeler Name	Amneal Pharmaceuticals NY LLC
Pharmaceutical Class	Phosphodiesterase 5 Inhibitor [EPC], Phosphodiesterase 5 Inhibitors [MoA]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA210738
Listing Certified Through	2024-12-31

Package

NDC 69238-1153-03 (69238115303)

Pricing Information	N/A
NDC Package Code	69238-1153-3
Billing NDC	69238115303
Package	30 TABLET, FILM COATED in 1 BOTTLE (69238-1153-3)
Marketing Start Date	2018-10-31
NDC Exclude Flag	N