NDC Package 42043-130-09 Naratriptan

View Billable Units, 11-Digit Format, RxNorm

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
42043-130-09
Package Description:
1 BLISTER PACK in 1 CARTON / 9 TABLET, FILM COATED in 1 BLISTER PACK (42043-130-00)
Product Code:
Proprietary Name:
Naratriptan
Usage Information:
Naratriptan tablets are indicated for the acute treatment of migraine with or without aura in adults.Limitations of Use:Use only if a clear diagnosis of migraine has been established. If a patient has no response to the first migraine attack treated with naratriptan tablets, reconsider the diagnosis of migraine before naratriptan tablets are administered to treat any subsequent attacks.Naratriptan tablets are not indicated for the prevention of migraine attacks.Safety and effectiveness of naratriptan tablets have not been established for cluster headache.
11-Digit NDC Billing Format:
42043013009
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
1 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 311918 - naratriptan 1 MG Oral Tablet
  • RxCUI: 311918 - naratriptan (as naratriptan hydrochloride) 1 MG Oral Tablet
  • RxCUI: 314135 - naratriptan 2.5 MG Oral Tablet
  • RxCUI: 314135 - naratriptan (as naratriptan hydrochloride) 2.5 MG Oral Tablet
  • Labeler Name:
    Orchidpharma, Inc
    Sample Package:
    No
    Start Marketing Date:
    12-12-2012
    Listing Expiration Date:
    12-31-2023
    Exclude Flag:
    I
    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 42043-130-09?

    The NDC Packaged Code 42043-130-09 is assigned to a package of 1 blister pack in 1 carton / 9 tablet, film coated in 1 blister pack (42043-130-00) of Naratriptan, labeled by Orchidpharma, Inc. The product's dosage form is and is administered via form.

    Is NDC 42043-130 included in the NDC Directory?

    No, Naratriptan with product code 42043-130 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Orchidpharma, Inc on December 12, 2012 and its listing in the NDC Directory is set to expire on December 31, 2023 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 42043-130-09?

    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 1.

    What is the 11-digit format for NDC 42043-130-09?

    The 11-digit format is 42043013009. 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
    5-3-242043-130-095-4-242043-0130-09