Rimantadine Hydrochloride Tablet, Film Coated
NDC Package 0115-1911-01
Package Information
Rimantadine Hydrochloride tablets is rimantadine hydrochloride tablet is indicated for the prophylaxis and treatment of illness caused by various strains of influenza A virus in adults (17 years and older). This formulation utilizes a tablet, film coated delivery system. Marketed by Amneal Pharmaceuticals Of New York Llc, this product is identified by NDC 0115-1911 and is authorized under FDA application ANDA076132.
Identification & Billing
- RxCUI: 856605 - riMANTAdine HCl 100 MG Oral Tablet
- RxCUI: 856605 - rimantadine hydrochloride 100 MG Oral Tablet
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 0115 - Amneal Pharmaceuticals Of New York Llc
- 0115-1911 - Rimantadine Hydrochloride
- 0115-1911-01 - 100 TABLET, FILM COATED in 1 BOTTLE
- 0115-1911 - Rimantadine Hydrochloride
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.
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Other Available Packages
The following commercial packages are registered under the same Product NDC (0115-1911). 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 0115-1911-01 identifies a specific commercial package of 100 tablet, film coated in 1 bottle of Rimantadine Hydrochloride, a human prescription drug labeled by Amneal Pharmaceuticals Of New York Llc. This product is billed for "EA" each discreet unit and contains an estimated amount of 100 billable units per package. This tablet, film coated is formulated for oral use and contains rimantadine hydrochloride as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Amneal Pharmaceuticals Of New York Llc on November 16, 2021. The current certification is valid through December 31, 2026.
How is this Amneal Pharmaceuticals Of New York Llc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 00115191101. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 100 total billable units per package. 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.