NDC 71335-1587 Tadalafil
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Product Packages
NDC Code 71335-1587-1
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE
NDC Code 71335-1587-2
Package Description: 10 TABLET, FILM COATED in 1 BOTTLE
NDC Code 71335-1587-3
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE
NDC Code 71335-1587-4
Package Description: 5 TABLET, FILM COATED in 1 BOTTLE
NDC Code 71335-1587-5
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE
NDC Code 71335-1587-6
Package Description: 20 TABLET, FILM COATED in 1 BOTTLE
NDC Code 71335-1587-7
Package Description: 15 TABLET, FILM COATED in 1 BOTTLE
Product Details
What is NDC 71335-1587?
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:
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- HYPROMELLOSE 2910 (6 MPA.S) (UNII: 0WZ8WG20P6)
- HYPROMELLOSE 2910 (3 MPA.S) (UNII: 0VUT3PMY82)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIACETIN (UNII: XHX3C3X673)
What is the NDC to RxNorm Crosswalk for Tadalafil?
- RxCUI: 402019 - tadalafil 20 MG Oral Tablet
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Patient Education
Tadalafil
Tadalafil (Cialis) is used to treat erectile dysfunction (ED, impotence; inability to get or keep an erection), and the symptoms of benign prostatic hyperplasia (BPH; an enlarged prostate) which include difficulty urinating (hesitation, dribbling, weak stream, and incomplete bladder emptying), painful urination, and urinary frequency and urgency in adult men. Tadalafil (Adcirca) is used to improve the ability to exercise in people with pulmonary arterial hypertension (PAH; high blood pressure in the vessels carrying blood to the lungs, causing shortness of breath, dizziness, and tiredness). Tadalafil is in a class of medications called phosphodiesterase (PDE) inhibitors. It works to treat erectile dysfunction by increasing blood flow to the penis during sexual stimulation. This increased blood flow can cause an erection. Tadalafil treats PAH by relaxing the blood vessels in the lungs to allow blood to flow more easily. If you are taking tadalafil to treat erectile dysfunction, you should know that it does not cure erectile dysfunction or increase sexual desire. Tadalafil 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.
[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".