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  5. NDC Package Code: 72030-001-01 Yinchiao

NDC Package 72030-001-01 Yinchiao

Acetaminophen And Chlorpheniramine Maleate Tablet, Coated Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. 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:
72030-001-01
Package Description:
120 TABLET, COATED in 1 BOTTLE
Product Code:
72030-001
Proprietary Name:
Yinchiao
Non-Proprietary Name:
Acetaminophen And Chlorpheniramine Maleate
Substance Name:
Acetaminophen; Chlorpheniramine Maleate
11-Digit NDC Billing Format:
72030000101
NDC to RxNorm Crosswalk:
  • RxCUI: 1599133 - acetaminophen 60 MG / chlorpheniramine maleate 0.667 MG Oral Tablet
  • RxCUI: 1599133 - APAP 60 MG / Chlorpheniramine Maleate 0.667 MG Oral Tablet
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Anhui Dongshengyoubang Pharmaceutical Co., Ltd.
    Dosage Form:
    Tablet, Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is covered with a designated coating.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • ACETAMINOPHEN 60 mg/1
  • CHLORPHENIRAMINE MALEATE .667 mg/1
    • Pharmacologic Class(es):
  • Histamine H1 Receptor Antagonists - [MoA] (Mechanism of Action)
  • Histamine-1 Receptor Antagonist - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    part341
    Marketing Category:
    OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
    Start Marketing Date:
    01-18-2018
    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.

    Frequently Asked Questions

    What is NDC 72030-001-01?

    The NDC Packaged Code 72030-001-01 is assigned to a package of 120 tablet, coated in 1 bottle of Yinchiao, a human over the counter drug labeled by Anhui Dongshengyoubang Pharmaceutical Co., Ltd.. The product's dosage form is tablet, coated and is administered via oral form.

    Is NDC 72030-001 included in the NDC Directory?

    Yes, Yinchiao with product code 72030-001 is active and included in the NDC Directory. The product was first marketed by Anhui Dongshengyoubang Pharmaceutical Co., Ltd. on January 18, 2018 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 72030-001-01?

    The 11-digit format is 72030000101. 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
    5-3-272030-001-015-4-272030-0001-01