Binosto
NDC Package 0178-0101-01
Package Information
Binosto is alendronate is used to prevent and treat certain types of bone loss (osteoporosis) in adults. Marketed by Mission Pharmacal Company, this product is identified by NDC 0178-0101 and is authorized under FDA application NDA202344.
Identification & Billing
- 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]
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 0178 - Mission Pharmacal Company
- 0178-0101 - Binosto
- 0178-0101-01 - 1 TABLET, EFFERVESCENT in 1 CARTON
- 0178-0101 - Binosto
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
* Please review the full disclaimer at the bottom of this page.
Other Available Packages
The following commercial packages are registered under the same Product NDC (0178-0101). Click a package code to view its specific billing and regulatory data.
* Please review the full disclaimer at the bottom of this page.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 0178-0101-01 identifies a specific commercial package of 1 tablet, effervescent in 1 carton of Binosto, labeled by Mission Pharmacal Company. This is formulated for use and contains as the active substance.
Is this product currently listed with the FDA?
This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Mission Pharmacal Company on September 03, 2012. The current certification is valid through December 31, 2019.
What are the primary indications for this medication?
Alendronate is used to prevent and treat certain types of bone loss (osteoporosis) in adults. Osteoporosis causes bones to become thinner and break more easily. Your chance of developing osteoporosis increases as you age, after menopause, or if you are taking corticosteroid medications (such as prednisone) for a long time. This medication works by slowing bone loss. This effect helps maintain strong bones and reduce the risk of broken bones (fractures). Alendronate belongs to a class of drugs called bisphosphonates.
How is this Mission Pharmacal Company product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 00178010101. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Labeler segment to maintain the 5-4-2 structure.