NDC Package 61990-0411-1 Dihydroergotamine Mesylate

Injection, Solution Intramuscular; Intravenous; Subcutaneous - 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:
61990-0411-1
Package Description:
5 AMPULE in 1 CARTON / 1 mL in 1 AMPULE (61990-0411-0)
Product Code:
Proprietary Name:
Dihydroergotamine Mesylate
Non-Proprietary Name:
Dihydroergotamine Mesylate
Substance Name:
Dihydroergotamine Mesylate
Usage Information:
This medication is used to treat migraine headache attacks. It helps relieve headache pain and other symptoms such as sensitivity to light or sound. Prompt treatment allows you to get back to your normal routine sooner and may decrease your need for other pain medications. This medication is not used to prevent migraines from occurring. Dihydroergotamine belongs to a class of drugs known as ergot alkaloids. It may work by narrowing the blood vessels in the brain. It may also block other pain pathways in the brain.
11-Digit NDC Billing Format:
61990041101
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 861672 - dihydroergotamine mesylate 1 MG in 1 ML Injection
  • RxCUI: 861672 - 1 ML dihydroergotamine mesylate 1 MG/ML Injection
  • RxCUI: 861672 - 1 ML DHE Mesylate 1 MG/ML Injection
  • RxCUI: 861672 - dihydroergotamine mesylate 1 MG per 1 ML Injection
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Apollo Pharmaceuticals Inc.
    Dosage Form:
    Injection, Solution - A liquid preparation containing one or more drug substances dissolved in a suitable solvent or mixture of mutually miscible solvents that is suitable for injection.
    Administration Route(s):
  • Intramuscular - Administration within a muscle.
  • Intravenous - Administration within or into a vein or veins.
  • Subcutaneous - Administration beneath the skin; hypodermic. Synonymous with the term SUBDERMAL.
  • Sample Package:
    No
    FDA Application Number:
    ANDA212046
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    04-14-2020
    End Marketing Date:
    03-31-2024
    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.

    NDC HCPCS Crosswalk

    This crosswalk is intended to help the public understand which drug products (identified by NDCs) are assigned to which HCPCS billing codes.

    NDC 61990-0411-1 HCPCS crosswalk information with package details and bill units information.

    NDC Billing CodeHCPCS CodeHCPCS Code Desc.DosagePackage SizePackage QuantityBillable UnitsBillable Units / Pkg
    61990041101J1110Inj dihydroergotamine mesylt1 MG1515

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    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    61990-0411-210 AMPULE in 1 CARTON / 1 mL in 1 AMPULE (61990-0411-0)

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    Frequently Asked Questions

    What is NDC 61990-0411-1?

    The NDC Packaged Code 61990-0411-1 is assigned to a package of 5 ampule in 1 carton / 1 ml in 1 ampule (61990-0411-0) of Dihydroergotamine Mesylate, a human prescription drug labeled by Apollo Pharmaceuticals Inc.. The product's dosage form is injection, solution and is administered via intramuscular; intravenous; subcutaneous form.

    Is NDC 61990-0411 included in the NDC Directory?

    Yes, Dihydroergotamine Mesylate with product code 61990-0411 is active and included in the NDC Directory. The product was first marketed by Apollo Pharmaceuticals Inc. on April 14, 2020.

    What is the NDC billing unit for package 61990-0411-1?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

    What is the 11-digit format for NDC 61990-0411-1?

    The 11-digit format is 61990041101. 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
    5-4-161990-0411-15-4-261990-0411-01