NDC 0178-0101 Binosto
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
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Product Details
What is NDC 0178-0101?
What are the uses for Binosto?
Which are Binosto UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALENDRONATE SODIUM (UNII: 2UY4M2U3RA)
- ALENDRONIC ACID (UNII: X1J18R4W8P) (Active Moiety)
Which are Binosto 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:
- MONOSODIUM CITRATE (UNII: 68538UP9SE)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- SODIUM CARBONATE (UNII: 45P3261C7T)
- ACESULFAME POTASSIUM (UNII: 23OV73Q5G9)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
What is the NDC to RxNorm Crosswalk for Binosto?
- RxCUI: 1248077 - alendronate sodium 70 MG Effervescent Oral Tablet
- RxCUI: 1248077 - alendronic acid 70 MG Effervescent Oral Tablet
- RxCUI: 1248077 - alendronic acid (as alendronate sodium) 70 MG Effervescent Oral Tablet
- RxCUI: 1248083 - Binosto 70 MG Effervescent Oral Tablet
- RxCUI: 1248083 - alendronic acid 70 MG Effervescent Oral Tablet [Binosto]
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Patient Education
Alendronate
Alendronate is used to treat and prevent osteoporosis (a condition in which the bones become thin and weak and break easily) in women who have undergone menopause (''change of life,'' end of menstrual periods) and to treat osteoporosis in men. Alendronate is also used to treat osteoporosis in men and women who are taking corticosteroids (a type of medication that may cause osteoporosis in some patients). Alendronate is also used to treat Paget's disease of bone (a condition in which the bones are soft and weak and may be deformed, painful, or easily broken). Alendronate is in a class of medications called bisphosphonates. It works by preventing bone breakdown and increasing bone density (thickness).
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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".