NDC 50771-014 Entecavir
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50771 - Yaopharma Co., Ltd.
- 50771-014 - Entecavir
Product Characteristics
10 MM
Y;14
Product Packages
NDC Code 50771-014-01
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE
Product Details
What is NDC 50771-014?
What are the uses for Entecavir?
Which are Entecavir UNII Codes?
The UNII codes for the active ingredients in this product are:
- ENTECAVIR (UNII: 5968Y6H45M)
- ENTECAVIR ANHYDROUS (UNII: NNU2O4609D) (Active Moiety)
Which are Entecavir 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:
- CROSPOVIDONE (UNII: 2S7830E561)
- HYPROMELLOSE 2910 (15 MPA.S) (UNII: 36SFW2JZ0W)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)
- POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Entecavir?
- RxCUI: 485434 - entecavir 0.5 MG Oral Tablet
- RxCUI: 485436 - entecavir 1 MG Oral Tablet
* Please review the disclaimer below.
Patient Education
Entecavir
Entecavir is used to treat chronic (long-term) hepatitis B infection (swelling of the liver caused by a virus) in adults and children 2 years of age and older who have liver damage. Entecavir is in a class of medications called nucleoside analogs. It works by decreasing the amount of hepatitis B virus (HBV) in the body. Entecavir does not cure HBV and may not prevent complications of chronic hepatitis B such as cirrhosis of the liver or liver cancer. Entecavir does not prevent the spread of HBV to other people.
[Learn More]
* 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".