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  5. NDC Package Code: 68462-121-05 Nicardipine Hydrochloride

NDC Package 68462-121-05 Nicardipine Hydrochloride

Capsule Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

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:
68462-121-05
Package Description:
500 CAPSULE in 1 BOTTLE
Product Code:
68462-121
Proprietary Name:
Nicardipine Hydrochloride
Non-Proprietary Name:
Nicardipine Hydrochloride
Substance Name:
Nicardipine Hydrochloride
Usage Information:
I. Stable AnginaNicardipine hydrochloride capsules are indicated for the management of patients with chronic stable angina (effort-associated angina). Nicardipine hydrochloride capsules may be used alone or in combination with beta-blockers.II. HypertensionNicardipine hydrochloride capsules are indicated for the treatment of hypertension. Nicardipine hydrochloride capsules may be used alone or in combination with other antihypertensive drugs. In administering nicardipine it is important to be aware of the relatively large peak to trough differences in blood pressure effect (see DOSAGE AND ADMINISTRATION).
11-Digit NDC Billing Format:
68462012105
NDC to RxNorm Crosswalk:
  • RxCUI: 858613 - niCARdipine HCl 20 MG Oral Capsule
  • RxCUI: 858613 - nicardipine hydrochloride 20 MG Oral Capsule
  • RxCUI: 858616 - niCARdipine HCl 30 MG Oral Capsule
  • RxCUI: 858616 - nicardipine hydrochloride 30 MG Oral Capsule
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Glenmark Pharmaceuticals Inc., Usa
    Dosage Form:
    Capsule - A solid oral dosage form consisting of a shell and a filling. The shell is composed of a single sealed enclosure, or two halves that fit together and which are sometimes sealed with a band. Capsule shells may be made from gelatin, starch, or cellulose, or other suitable materials, may be soft or hard, and are filled with solid or liquid ingredients that can be poured or squeezed.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • NICARDIPINE HYDROCHLORIDE 30 mg/1
    • Pharmacologic Class(es):
  • Calcium Channel Antagonists - [MoA] (Mechanism of Action)
  • Cytochrome P450 2C19 Inhibitors - [MoA] (Mechanism of Action)
  • Cytochrome P450 2C8 Inhibitors - [MoA] (Mechanism of Action)
  • Cytochrome P450 2D6 Inhibitors - [MoA] (Mechanism of Action)
  • Cytochrome P450 3A4 Inhibitors - [MoA] (Mechanism of Action)
  • Dihydropyridine Calcium Channel Blocker - [EPC] (Established Pharmacologic Class)
  • Dihydropyridines - [CS]
    • Sample Package:
    No
    FDA Application Number:
    ANDA216357
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    12-16-2022
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    68462-121-9090 CAPSULE in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 68462-121-05?

    The NDC Packaged Code 68462-121-05 is assigned to a package of 500 capsule in 1 bottle of Nicardipine Hydrochloride, a human prescription drug labeled by Glenmark Pharmaceuticals Inc., Usa. The product's dosage form is capsule and is administered via oral form.

    Is NDC 68462-121 included in the NDC Directory?

    Yes, Nicardipine Hydrochloride with product code 68462-121 is active and included in the NDC Directory. The product was first marketed by Glenmark Pharmaceuticals Inc., Usa on December 16, 2022 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 68462-121-05?

    The 11-digit format is 68462012105. 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
    5-3-268462-121-055-4-268462-0121-05