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  5. NDC Package Code: 71335-0736-6 Morphine Sulfate

NDC Package 71335-0736-6 Morphine Sulfate

Tablet, Film Coated, Extended Release 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:
71335-0736-6
Package Description:
14 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
Product Code:
71335-0736
Proprietary Name:
Morphine Sulfate
Non-Proprietary Name:
Morphine Sulfate
Substance Name:
Morphine Sulfate
Usage Information:
This medication is used to treat severe pain. Morphine belongs to a class of drugs known as opioid analgesics. It works in the brain to change how your body feels and responds to pain.
11-Digit NDC Billing Format:
71335073606
NDC to RxNorm Crosswalk:
  • RxCUI: 891881 - morphine sulfate 15 MG Extended Release Oral Tablet
  • RxCUI: 891881 - MS 15 MG Extended Release Oral Tablet
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Bryant Ranch Prepack
    Dosage Form:
    Tablet, Film Coated, Extended Release - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer; the tablet is formulated in such manner as to make the contained medicament available over an extended period of time following ingestion.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • MORPHINE SULFATE 15 mg/1
    • Pharmacologic Class(es):
  • Full Opioid Agonists - [MoA] (Mechanism of Action)
  • Opioid Agonist - [EPC] (Established Pharmacologic Class)
    • DEA Schedule:
    Schedule II (CII) Substances
    Sample Package:
    No
    FDA Application Number:
    ANDA078761
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    05-11-2012
    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
    71335-0736-026 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
    71335-0736-130 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
    71335-0736-260 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
    71335-0736-390 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
    71335-0736-4120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
    71335-0736-540 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
    71335-0736-715 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
    71335-0736-820 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
    71335-0736-984 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 71335-0736-6?

    The NDC Packaged Code 71335-0736-6 is assigned to a package of 14 tablet, film coated, extended release in 1 bottle of Morphine Sulfate, a human prescription drug labeled by Bryant Ranch Prepack. The product's dosage form is tablet, film coated, extended release and is administered via oral form.

    Is NDC 71335-0736 included in the NDC Directory?

    Yes, Morphine Sulfate with product code 71335-0736 is active and included in the NDC Directory. The product was first marketed by Bryant Ranch Prepack on May 11, 2012 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 71335-0736-6?

    The 11-digit format is 71335073606. 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
    5-4-171335-0736-65-4-271335-0736-06