NDC 33342-153 Vardenafil Hydrochloride
Tablet Oral - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 33342 - Macleods Pharmaceuticals Limited
- 33342-153 - Vardenafil Hydrochloride
Product Characteristics
ORANGE (C48331)
7 MM
L51
L52
Product Packages
NDC Code 33342-153-11
Package Description: 100 TABLET in 1 BOTTLE
NDC Code 33342-153-12
Package Description: 10 BLISTER PACK in 1 CARTON / 10 TABLET in 1 BLISTER PACK
Product Details
What is NDC 33342-153?
What are the uses for Vardenafil Hydrochloride?
What are Vardenafil Hydrochloride Active Ingredients?
- VARDENAFIL 10 mg/1 - A piperazine derivative, PHOSPHODIESTERASE 5 INHIBITOR and VASODILATOR AGENT that is used as a UROLOGICAL AGENT in the treatment of ERECTILE DYSFUNCTION.
Which are Vardenafil Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- VARDENAFIL (UNII: UCE6F4125H)
- VARDENAFIL (UNII: UCE6F4125H) (Active Moiety)
Which are Vardenafil Hydrochloride Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- CROSPOVIDONE (UNII: 68401960MK)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
What is the NDC to RxNorm Crosswalk for Vardenafil Hydrochloride?
- RxCUI: 349478 - vardenafil 5 MG Oral Tablet
- RxCUI: 349478 - vardenafil 5 MG (vardenafil hydrochloride 5.926 MG) Oral Tablet
- RxCUI: 349479 - vardenafil HCl 10 MG Oral Tablet
- RxCUI: 349479 - vardenafil 10 MG Oral Tablet
- RxCUI: 349479 - vardenafil 10 MG (vardenafil HCl 11.85 MG) Oral Tablet
Which are the Pharmacologic Classes for Vardenafil Hydrochloride?
* Please review the disclaimer below.
Patient Education
Vardenafil
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).
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* Please review the disclaimer below.
[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
[2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".