NDC Package 51467-005-01 Coltalin

Acetaminophen,Chlorpheniramine Maleate,Phenylephrine Hydrochloride Tablet 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:
51467-005-01
Package Description:
2 BLISTER PACK in 1 BOX / 12 TABLET in 1 BLISTER PACK
Product Code:
Proprietary Name:
Coltalin
Non-Proprietary Name:
Acetaminophen, Chlorpheniramine Maleate, Phenylephrine Hydrochloride
Substance Name:
Acetaminophen; Chlorpheniramine Maleate; Phenylephrine Hydrochloride
Usage Information:
Usestemporarily relieves these symptoms due to a cold, the flu, or hay fever:     minor aches and pains      sore throat     headache     sinus congestion and pressure     nasal congestion     runny nose     sneezing, itching of the nose or throat, and itchy, watery eyestemporarily reduces feverpromotes nasal and/or sinus drainage
11-Digit NDC Billing Format:
51467000501
NDC to RxNorm Crosswalk:
  • RxCUI: 1046781 - acetaminophen 325 MG / chlorpheniramine maleate 2 MG / phenylephrine HCl 5 MG Oral Tablet
  • RxCUI: 1046781 - acetaminophen 325 MG / chlorpheniramine maleate 2 MG / phenylephrine hydrochloride 5 MG Oral Tablet
  • RxCUI: 1046781 - APAP 325 MG / chlorpheniramine maleate 2 MG / phenylephrine hydrochloride 5 MG Oral Tablet
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Fortune Pharmacal Company Limited
    Dosage Form:
    Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    FDA Application Number:
    M
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    03-01-2004
    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
    51467-005-023 BLISTER PACK in 1 BOX / 12 TABLET in 1 BLISTER PACK

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 51467-005-01?

    The NDC Packaged Code 51467-005-01 is assigned to a package of 2 blister pack in 1 box / 12 tablet in 1 blister pack of Coltalin, a human over the counter drug labeled by Fortune Pharmacal Company Limited. The product's dosage form is tablet and is administered via oral form.

    Is NDC 51467-005 included in the NDC Directory?

    Yes, Coltalin with product code 51467-005 is active and included in the NDC Directory. The product was first marketed by Fortune Pharmacal Company Limited on March 01, 2004 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 51467-005-01?

    The 11-digit format is 51467000501. 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
    5-3-251467-005-015-4-251467-0005-01