NDC 50436-1120 Tadalafil
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50436 - Unit Dose Services
- 50436-1120 - Tadalafil
Product Characteristics
Product Packages
NDC Code 50436-1120-1
Package Description: 200 POUCH in 1 CASE / 1 TABLET in 1 POUCH
Product Details
What is NDC 50436-1120?
What are the uses for Tadalafil?
Which are Tadalafil UNII Codes?
The UNII codes for the active ingredients in this product are:
- TADALAFIL (UNII: 742SXX0ICT)
- TADALAFIL (UNII: 742SXX0ICT) (Active Moiety)
Which are Tadalafil 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:
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- LOW-SUBSTITUTED HYDROXYPROPYL CELLULOSE (11% HYDROXYPROPYL; 100000 MW) (UNII: BMJ7J4127K)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- TRIACETIN (UNII: XHX3C3X673)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- ALUMINUM OXIDE (UNII: LMI26O6933)
What is the NDC to RxNorm Crosswalk for Tadalafil?
- RxCUI: 402019 - tadalafil 20 MG Oral Tablet
- RxCUI: 403957 - tadalafil 5 MG Oral Tablet
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Patient Education
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Mupirocin, an antibiotic, is used to treat impetigo as well as other skin infections caused by bacteria. It is not effective against fungal or viral infections. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
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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".