vardenafil hydrochloride
Generic: vardenafil hydrochloride
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
vardenafil hydrochloride
Generic Name
vardenafil hydrochloride
Labeler
bryant ranch prepack
Dosage Form
TABLET
Routes
Active Ingredients
vardenafil hydrochloride 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-9696
Product ID
71335-9696_c4b53c3e-e0c7-4368-beda-8c27a32ad5c9
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA209057
Listing Expiration
2026-12-31
Marketing Start
2018-11-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713359696
Hyphenated Format
71335-9696
Supplemental Identifiers
RxCUI
UNII
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
ANDA209057 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (71335-9696-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c4b53c3e-e0c7-4368-beda-8c27a32ad5c9", "openfda": {"unii": ["5M8S2CU0TS"], "rxcui": ["349479"], "spl_set_id": ["8791997d-3b86-45af-988f-808e259da506"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-9696-1)", "package_ndc": "71335-9696-1", "marketing_start_date": "20230412"}], "brand_name": "Vardenafil Hydrochloride", "product_id": "71335-9696_c4b53c3e-e0c7-4368-beda-8c27a32ad5c9", "dosage_form": "TABLET", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "71335-9696", "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": "10 mg/1"}], "application_number": "ANDA209057", "marketing_category": "ANDA", "marketing_start_date": "20181101", "listing_expiration_date": "20261231"}