NDC Package 35781-0600-8 Rizafilm

Rizatriptan Benzoate Film Oral - View Billable Units, 11-Digit Format, RxNorm

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
35781-0600-8
Package Description:
18 POUCH in 1 CARTON / 1 FILM in 1 POUCH (35781-0600-1)
Product Code:
Proprietary Name:
Rizafilm
Non-Proprietary Name:
Rizatriptan Benzoate
Substance Name:
Rizatriptan Benzoate
Usage Information:
Rizatriptan is used to treat migraines. It helps to relieve headache, pain, and other migraine symptoms (including nausea, vomiting, sensitivity to light/sound). Prompt treatment helps you return to your normal routine and may decrease your need for other pain medications. Rizatriptan belongs to a class of drugs known as triptans. It affects a certain natural substance (serotonin) that causes narrowing of blood vessels in the brain. It may also relieve pain by affecting certain nerves in the brain. Rizatriptan does not prevent future migraines or lessen how often you get migraine attacks.
11-Digit NDC Billing Format:
35781060008
NDC to RxNorm Crosswalk:
  • RxCUI: 2634482 - rizatriptan 10 MG Oral Film
  • RxCUI: 2634482 - rizatriptan 10 MG (as rizatriptan benzoate 14.53 MG) Oral Film
  • RxCUI: 2672955 - RizaFilm 10 MG Oral Film
  • RxCUI: 2672955 - rizatriptan 10 MG Oral Film [Rizafilm]
  • RxCUI: 2672955 - RizaFilm 10 MG (as rizatriptan benzoate 14.53 MG) Oral Film
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Gensco Laboratories Llc
    Dosage Form:
    Film - A thin layer or coating.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    NDA205394
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    01-10-2024
    Listing Expiration Date:
    12-31-2025
    Exclude Flag:
    N
    Code Structure:

    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 disclaimer below.

    Frequently Asked Questions

    What is NDC 35781-0600-8?

    The NDC Packaged Code 35781-0600-8 is assigned to a package of 18 pouch in 1 carton / 1 film in 1 pouch (35781-0600-1) of Rizafilm, a human prescription drug labeled by Gensco Laboratories Llc. The product's dosage form is film and is administered via oral form.

    Is NDC 35781-0600 included in the NDC Directory?

    Yes, Rizafilm with product code 35781-0600 is active and included in the NDC Directory. The product was first marketed by Gensco Laboratories Llc on January 10, 2024 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 35781-0600-8?

    The 11-digit format is 35781060008. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-4-1 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-4-135781-0600-85-4-235781-0600-08