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  5. NDC Package Code: 35208-011-10 Venlafaxine Hydrochloride

NDC Package 35208-011-10 Venlafaxine Hydrochloride

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
35208-011-10
Package Description:
1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE
Product Code:
35208-011
Proprietary Name:
Venlafaxine Hydrochloride
Usage Information:
Venlafaxine Hydrochloride Extended-release Capsules is indicated for the treatment of major depressive disorder (MDD). Efficacy was established in three short-term (4, 8, and 12 weeks) and two long-term, maintenance trials.
11-Digit NDC Billing Format:
35208001110
NDC to RxNorm Crosswalk:
  • RxCUI: 313581 - venlafaxine HCl 150 MG 24HR Extended Release Oral Capsule
  • RxCUI: 313581 - 24 HR venlafaxine 150 MG Extended Release Oral Capsule
  • RxCUI: 313581 - venlafaxine (as venlafaxine HCl) 150 MG 24 HR Extended Release Oral Capsule
  • RxCUI: 313583 - venlafaxine HCl 37.5 MG 24HR Extended Release Oral Capsule
  • RxCUI: 313583 - 24 HR venlafaxine 37.5 MG Extended Release Oral Capsule
    • Labeler Name:
    Intellipharmaceutics Corp.
    Sample Package:
    No
    Start Marketing Date:
    12-03-2018
    Listing Expiration Date:
    12-31-2019
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    35208-011-1515 CAPSULE, EXTENDED RELEASE in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 35208-011-10?

    The NDC Packaged Code 35208-011-10 is assigned to a package of 1000 capsule, extended release in 1 bottle of Venlafaxine Hydrochloride, labeled by Intellipharmaceutics Corp.. The product's dosage form is and is administered via form.

    Is NDC 35208-011 included in the NDC Directory?

    No, Venlafaxine Hydrochloride with product code 35208-011 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Intellipharmaceutics Corp. on December 03, 2018 and its listing in the NDC Directory is set to expire on December 31, 2019 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 35208-011-10?

    The 11-digit format is 35208001110. 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
    5-3-235208-011-105-4-235208-0011-10