NDC Package 47335-618-10 Drizalma Sprinkle

Duloxetine Capsule, Delayed Release Oral - 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:
47335-618-10
Package Description:
1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE
Product Code:
Proprietary Name:
Drizalma Sprinkle
Non-Proprietary Name:
Duloxetine
Substance Name:
Duloxetine Hydrochloride
Usage Information:
Duloxetine is used to treat depression and anxiety. It is also used to help relieve nerve pain (peripheral neuropathy) in people with diabetes or ongoing pain due to medical conditions such as arthritis or chronic back pain. Duloxetine may improve your mood, sleep, appetite, and energy level, and decrease nervousness. It can also decrease pain due to certain medical conditions. Duloxetine is known as a serotonin-norepinephrine reuptake inhibitor (SNRI). This medication works by helping to restore the balance of certain natural substances (serotonin and norepinephrine) in the brain.
11-Digit NDC Billing Format:
47335061810
NDC to RxNorm Crosswalk:
  • RxCUI: 2200168 - DULoxetine 20 MG Sprinkle Delayed Release Oral Capsule
  • RxCUI: 2200168 - Sprinkle duloxetine 20 MG Delayed Release Oral Capsule
  • RxCUI: 2200168 - duloxetine 20 MG Sprinkle (as duloxetine HCl 22.4 MG) Delayed Release Oral Capsule
  • RxCUI: 2200174 - DRIZALMA 20 MG Delayed Release Oral Capsule
  • RxCUI: 2200174 - Sprinkle duloxetine 20 MG Delayed Release Oral Capsule [Drizalma]
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Sun Pharmaceutical Industries, Inc.
    Dosage Form:
    Capsule, Delayed Release - A solid dosage form in which the drug is enclosed within either a hard or soft soluble container made from a suitable form of gelatin, and which releases a drug (or drugs) at a time other than promptly after administration. Enteric-coated articles are delayed release dosage forms.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    NDA212516
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    08-01-2019
    Listing Expiration Date:
    12-31-2024
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    47335-618-3030 CAPSULE, DELAYED RELEASE in 1 BOTTLE
    47335-618-6060 CAPSULE, DELAYED RELEASE in 1 BOTTLE
    47335-618-9090 CAPSULE, DELAYED RELEASE in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 47335-618-10?

    The NDC Packaged Code 47335-618-10 is assigned to a package of 1000 capsule, delayed release in 1 bottle of Drizalma Sprinkle, a human prescription drug labeled by Sun Pharmaceutical Industries, Inc.. The product's dosage form is capsule, delayed release and is administered via oral form.

    Is NDC 47335-618 included in the NDC Directory?

    Yes, Drizalma Sprinkle with product code 47335-618 is active and included in the NDC Directory. The product was first marketed by Sun Pharmaceutical Industries, Inc. on August 01, 2019 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 47335-618-10?

    The 11-digit format is 47335061810. 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
    5-3-247335-618-105-4-247335-0618-10