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  5. NDC Package Code: 50419-482-03 Angeliq

NDC Package 50419-482-03 Angeliq

Drospirenone And Estradiol Tablet, Film Coated 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:
50419-482-03
Package Description:
3 BLISTER PACK in 1 CARTON / 28 TABLET, FILM COATED in 1 BLISTER PACK (50419-482-01)
Product Code:
50419-482
Proprietary Name:
Angeliq
Non-Proprietary Name:
Drospirenone And Estradiol
Substance Name:
Drospirenone; Estradiol
Usage Information:
This medication is used to reduce menopause symptoms. It helps reduce episodes of flushing and sweating of the upper body and face, commonly called hot flashes. It also helps treat dryness, itching, and burning around the vagina. These symptoms occur when a woman's body no longer makes the usual amount of female hormone (estrogen). This medication is a combination of 2 types of female hormones: an estrogen (estradiol) and a progestin (drospirenone). A progestin is added to estrogen replacement therapy to reduce the risk of cancer of the uterus. A woman who has had her uterus removed does not need progestin and should not be treated with this combination medication. If you need treatment only for vaginal menopause symptoms, products applied directly inside the vagina should be considered before medications that are taken by mouth, absorbed through the skin, or injected.
11-Digit NDC Billing Format:
50419048203
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
3 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 1483549 - drospirenone 0.25 MG / estradiol 0.5 MG Oral Tablet
  • RxCUI: 1483550 - {28 (drospirenone 0.25 MG / estradiol 0.5 MG Oral Tablet) } Pack
  • RxCUI: 1483550 - Drospiren-Estra 0.25-0.5 (28) Oral Tablet 28 Day Pack
  • RxCUI: 1483551 - {28 (drospirenone 0.25 MG / estradiol 0.5 MG Oral Tablet) } Pack [Angeliq 0.25/0.5 28 Day]
  • RxCUI: 1483551 - Angeliq 0.25/0.5 28 Day Pack
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Bayer Healthcare Pharmaceuticals Inc.
    Dosage Form:
    Tablet, Film Coated - 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.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • DROSPIRENONE .25 mg/1
  • ESTRADIOL .5 mg/1
    • Pharmacologic Class(es):
  • Estradiol Congeners - [CS]
  • Estrogen Receptor Agonists - [MoA] (Mechanism of Action)
  • Estrogen - [EPC] (Established Pharmacologic Class)
  • Progesterone Congeners - [CS]
  • Progestin - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    NDA021355
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    02-29-2012
    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
    50419-482-721 BLISTER PACK in 1 CARTON / 14 TABLET, FILM COATED in 1 BLISTER PACK (50419-482-71)

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 50419-482-03?

    The NDC Packaged Code 50419-482-03 is assigned to a package of 3 blister pack in 1 carton / 28 tablet, film coated in 1 blister pack (50419-482-01) of Angeliq, a human prescription drug labeled by Bayer Healthcare Pharmaceuticals Inc.. The product's dosage form is tablet, film coated and is administered via oral form.This product is billed for "EA" each discreet unit and contains an estimated amount of 3 billable units per package.

    Is NDC 50419-482 included in the NDC Directory?

    Yes, Angeliq with product code 50419-482 is active and included in the NDC Directory. The product was first marketed by Bayer Healthcare Pharmaceuticals Inc. on February 29, 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 NDC billing unit for package 50419-482-03?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 3.

    What is the 11-digit format for NDC 50419-482-03?

    The 11-digit format is 50419048203. 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
    5-3-250419-482-035-4-250419-0482-03