NDC Package 45737-240-02 Bio-g-tuss Pediatric Drops

Dextromethorphan Hbr,Guaifenesin,Phenylephrine Hcl Solution/ Drops 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:
45737-240-02
Package Description:
60 mL in 1 BOTTLE, DROPPER
Product Code:
Proprietary Name:
Bio-g-tuss Pediatric Drops
Non-Proprietary Name:
Dextromethorphan Hbr, Guaifenesin, Phenylephrine Hcl
Substance Name:
Dextromethorphan Hydrobromide; Guaifenesin; Phenylephrine Hydrochloride
Usage Information:
 AgeDose  children 6 to under 12 years of age2 mL every 6-8 hours  chidren 2 to under 6 years of age1 mL every 6-8 hours  children under 2 years of ageconsult a doctor 
11-Digit NDC Billing Format:
45737024002
NDC to RxNorm Crosswalk:
  • RxCUI: 1487369 - dextromethorphan HBr 7.5 MG / guaiFENesin 88 MG / phenylephrine HCl 2.5 MG in 1 mL Oral Solution
  • RxCUI: 1487369 - dextromethorphan hydrobromide 7.5 MG/ML / guaifenesin 88 MG/ML / phenylephrine hydrochloride 2.5 MG/ML Oral Solution
  • RxCUI: 1487369 - dextromethorphan HBr 7.5 MG/ML / guaifenesin 88 MG/ML / phenylephrine HCl 2.5 MG/ML Oral Solution
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Advanced Generic Corporation
    Dosage Form:
    Solution/ Drops - A solution which is usually administered in a drop-wise fashion.
    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:
    04-01-2016
    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.

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    Frequently Asked Questions

    What is NDC 45737-240-02?

    The NDC Packaged Code 45737-240-02 is assigned to a package of 60 ml in 1 bottle, dropper of Bio-g-tuss Pediatric Drops, a human over the counter drug labeled by Advanced Generic Corporation. The product's dosage form is solution/ drops and is administered via oral form.

    Is NDC 45737-240 included in the NDC Directory?

    Yes, Bio-g-tuss Pediatric Drops with product code 45737-240 is active and included in the NDC Directory. The product was first marketed by Advanced Generic Corporation on April 01, 2016 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 45737-240-02?

    The 11-digit format is 45737024002. 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
    5-3-245737-240-025-4-245737-0240-02