NDC 43353-744 Levitra
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43353 - Aphena Pharma Solutions - Tennessee, Inc.
- 43353-744 - Levitra
Product Characteristics
Product Packages
NDC Code 43353-744-02
Package Description: 2 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
NDC Code 43353-744-06
Package Description: 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product Details
What is NDC 43353-744?
What are the uses for Levitra?
Which are Levitra UNII Codes?
The UNII codes for the active ingredients in this product are:
- VARDENAFIL HYDROCHLORIDE (UNII: 5M8S2CU0TS)
- VARDENAFIL (UNII: UCE6F4125H) (Active Moiety)
Which are Levitra 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 (UNII: 3WJQ0SDW1A)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
What is the NDC to RxNorm Crosswalk for Levitra?
- 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
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[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".