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  5. NDC Package Code: 68405-037-36 Hypertenipine

NDC Package 68405-037-36 Hypertenipine

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
68405-037-36
Package Description:
1 KIT in 1 KIT * 90 CAPSULE in 1 BOTTLE * 30 TABLET in 1 BOTTLE (52959-910-30)
Product Code:
68405-037
Proprietary Name:
Hypertenipine
Usage Information:
INDICATIONS AND USAGE1. HypertensionAmlodipine besylate is indicated for the treatment of hypertension. It may be used alone or incombination with other antihypertensive agents.2. Coronary Artery DiseaseCronic Stable AnginaAmlodipine besylate is indicated for the symptomatic treatment of chronic stable angina.Amlodipine besylate may be used alone or in combination with other antianginal agents.Vasospastic Angina (Prinzmetal’s or Variant Angina)Amlodipine besylate is indicated for the treatment of confirmed or suspected vasospastic angina.Amlodipine besylate may be used as monotherapy or in combination with other antianginal drugs. INDICATIONS FOR USE  Hypertensa is intended for the clinical dietary management of the metabolic processes in patients with hypertension.
11-Digit NDC Billing Format:
68405003736
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
  • RxCUI: 308136 - amLODIPine besylate 2.5 MG Oral Tablet
  • RxCUI: 308136 - amlodipine 2.5 MG Oral Tablet
  • RxCUI: 308136 - amlodipine (as amlodipine besylate) 2.5 MG Oral Tablet
    • Labeler Name:
    Physician Therapeutics Llc
    Sample Package:
    No
    Start Marketing Date:
    07-07-2011
    Listing Expiration Date:
    12-31-2017
    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 68405-037-36?

    The NDC Packaged Code 68405-037-36 is assigned to a package of 1 kit in 1 kit * 90 capsule in 1 bottle * 30 tablet in 1 bottle (52959-910-30) of Hypertenipine, labeled by Physician Therapeutics Llc. The product's dosage form is and is administered via form.

    Is NDC 68405-037 included in the NDC Directory?

    No, Hypertenipine with product code 68405-037 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Physician Therapeutics Llc on July 07, 2011 and its listing in the NDC Directory is set to expire on December 31, 2017 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 68405-037-36?

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

    What is the 11-digit format for NDC 68405-037-36?

    The 11-digit format is 68405003736. 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
    5-3-268405-037-365-4-268405-0037-36