NDC Package 45737-205-16 Biogtuss

Dextromethorphan,Guaifenesin,Phenylephrine Liquid 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:
45737-205-16
Package Description:
473 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Biogtuss
Non-Proprietary Name:
Dextromethorphan, Guaifenesin, Phenylephrine
Substance Name:
Dextromethorphan Hydrobromide; Guaifenesin; Phenylephrine Hydrochloride
Usage Information:
Other information  store at room temperature 15°- 30°C (59° - 86°F).Tamper Evident Feature: Do not use if seal under cap (or cello-band over cap) is torn, broken or missing.Warning:Phenylketonuric. Contains 17 mg of Phenylalanine per 5 mL (one teaspoonful dose).
11-Digit NDC Billing Format:
45737020516
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
473 ML
Product Type:
Human Otc Drug
Labeler Name:
Advanced Generic Corporation
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • 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:
    10-01-2009
    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 45737-205-16?

    The NDC Packaged Code 45737-205-16 is assigned to a package of 473 ml in 1 bottle of Biogtuss, a human over the counter drug labeled by Advanced Generic Corporation. The product's dosage form is liquid and is administered via oral form.This product is billed per "ML" milliliter and contains an estimated amount of 473 billable units per package.

    Is NDC 45737-205 included in the NDC Directory?

    Yes, Biogtuss with product code 45737-205 is active and included in the NDC Directory. The product was first marketed by Advanced Generic Corporation on October 01, 2009 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 NDC billing unit for package 45737-205-16?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume. The calculated billable units for this package is 473.

    What is the 11-digit format for NDC 45737-205-16?

    The 11-digit format is 45737020516. 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
    5-3-245737-205-165-4-245737-0205-16