vardenafil hydrochloride

Generic: vardenafil hydrochloride

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name vardenafil hydrochloride
Generic Name vardenafil hydrochloride
Labeler bryant ranch prepack
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

vardenafil hydrochloride 20 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-2357
Product ID 71335-2357_d372a596-aa3a-4bd7-b311-ee32b051d758
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214031
Listing Expiration 2026-12-31
Marketing Start 2020-08-05

Pharmacologic Class

Classes
phosphodiesterase 5 inhibitor [epc] phosphodiesterase 5 inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713352357
Hyphenated Format 71335-2357

Supplemental Identifiers

RxCUI
349480
UNII
5M8S2CU0TS

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name vardenafil hydrochloride (source: ndc)
Generic Name vardenafil hydrochloride (source: ndc)
Application Number ANDA214031 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (71335-2357-1)
source: ndc

Packages (1)

71335-2357-1 30 TABLET, FILM COATED in 1 BOTTLE (71335-2357-1)

Ingredients (1)

vardenafil hydrochloride (20 mg/1)

Linked Drug Pages (1)

VARDENAFIL HYDROCHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d372a596-aa3a-4bd7-b311-ee32b051d758", "openfda": {"unii": ["5M8S2CU0TS"], "rxcui": ["349480"], "spl_set_id": ["d8a5cc4b-9d9d-43af-9ee4-57381aa6368a"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-2357-1)", "package_ndc": "71335-2357-1", "marketing_start_date": "20240528"}], "brand_name": "VARDENAFIL HYDROCHLORIDE", "product_id": "71335-2357_d372a596-aa3a-4bd7-b311-ee32b051d758", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "71335-2357", "generic_name": "VARDENAFIL HYDROCHLORIDE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VARDENAFIL HYDROCHLORIDE", "active_ingredients": [{"name": "VARDENAFIL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA214031", "marketing_category": "ANDA", "marketing_start_date": "20200805", "listing_expiration_date": "20261231"}