NDC 50436-0185 Sildenafil Citrate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50436 - Unit Dose Services
- 50436-0185 - Sildenafil Citrate
Product Characteristics
Product Packages
NDC Code 50436-0185-1
Package Description: 200 POUCH in 1 CASE / 3 TABLET in 1 POUCH
NDC Code 50436-0185-2
Package Description: 200 POUCH in 1 CASE / 4 TABLET in 1 POUCH
NDC Code 50436-0185-3
Package Description: 200 POUCH in 1 CASE / 5 TABLET in 1 POUCH
Product Details
What is NDC 50436-0185?
What are the uses for Sildenafil Citrate?
Which are Sildenafil Citrate UNII Codes?
The UNII codes for the active ingredients in this product are:
- SILDENAFIL CITRATE (UNII: BW9B0ZE037)
- SILDENAFIL (UNII: 3M7OB98Y7H) (Active Moiety)
Which are Sildenafil Citrate 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:
- ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- HYPROMELLOSE 2910 (6 MPA.S) (UNII: 0WZ8WG20P6)
- SODIUM STEARYL FUMARATE (UNII: 7CV7WJK4UI)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIACETIN (UNII: XHX3C3X673)
What is the NDC to RxNorm Crosswalk for Sildenafil Citrate?
- RxCUI: 577033 - sildenafil citrate 20 MG Oral Tablet
- RxCUI: 577033 - sildenafil 20 MG Oral Tablet
- RxCUI: 577033 - sildenafil 20 MG (as sildenafil citrate) Oral Tablet
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[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".