NDC Package 52427-803-90 Gralise

Gabapentin Tablet, Film Coated 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:
52427-803-90
Package Description:
90 TABLET, FILM COATED in 1 BOTTLE
Product Code:
Proprietary Name:
Gralise
Non-Proprietary Name:
Gabapentin
Substance Name:
Gabapentin
Usage Information:
This medication is used to relieve nerve pain following shingles (a painful rash due to herpes zoster infection) in adults. This condition is called postherpetic neuralgia. Gabapentin belongs to a class of drugs known as antiseizure drugs (also called anticonvulsant or antiepileptic drugs).
11-Digit NDC Billing Format:
52427080390
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
90 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 1115012 - Gralise 300 MG Once-Daily Oral Tablet
  • RxCUI: 1115012 - Once-Daily gabapentin 300 MG Oral Tablet [Gralise]
  • RxCUI: 1115012 - Once-Daily Gralise 300 MG Oral Tablet
  • RxCUI: 1115013 - Gralise 600 MG Once-Daily Oral Tablet
  • RxCUI: 1115013 - Once-Daily gabapentin 600 MG Oral Tablet [Gralise]
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Almatica Pharma Llc
    Dosage Form:
    Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    NDA022544
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    10-01-2020
    Listing Expiration Date:
    12-31-2024
    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 52427-803-90?

    The NDC Packaged Code 52427-803-90 is assigned to a package of 90 tablet, film coated in 1 bottle of Gralise, a human prescription drug labeled by Almatica Pharma Llc. The product's dosage form is tablet, film coated and is administered via oral form.

    Is NDC 52427-803 included in the NDC Directory?

    Yes, Gralise with product code 52427-803 is active and included in the NDC Directory. The product was first marketed by Almatica Pharma Llc on October 01, 2020 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 52427-803-90?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 90.

    What is the 11-digit format for NDC 52427-803-90?

    The 11-digit format is 52427080390. 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 5-3-2 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
    5-3-252427-803-905-4-252427-0803-90