NDC Package 63548-0739-3 Indoor Outdoor Allergies

Cetirizine Hcl 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:
63548-0739-3
Package Description:
1 BOTTLE, PLASTIC in 1 BOX / 300 TABLET in 1 BOTTLE, PLASTIC
Product Code:
Proprietary Name:
Indoor Outdoor Allergies
Non-Proprietary Name:
Cetirizine Hcl
Substance Name:
Cetirizine Hydrochloride
Usage Information:
Cetirizine is an antihistamine used to relieve allergy symptoms such as watery eyes, runny nose, itching eyes/nose, sneezing, hives, and itching. It works by blocking a certain natural substance (histamine) that your body makes during an allergic reaction. Cetirizine does not prevent hives or prevent/treat a serious allergic reaction (such as anaphylaxis). Therefore, if your doctor has prescribed epinephrine to treat allergic reactions, always carry your epinephrine injector with you. Do not use cetirizine in place of your epinephrine.
11-Digit NDC Billing Format:
63548073903
NDC to RxNorm Crosswalk:
  • RxCUI: 1014678 - cetirizine HCl 10 MG Oral Tablet
  • RxCUI: 1014678 - cetirizine hydrochloride 10 MG Oral Tablet
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Pld Acquisitions Llc Dba Av�ma Pharma Solutions
    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.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA077946
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    07-01-2019
    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 63548-0739-3?

    The NDC Packaged Code 63548-0739-3 is assigned to a package of 1 bottle, plastic in 1 box / 300 tablet in 1 bottle, plastic of Indoor Outdoor Allergies, a human over the counter drug labeled by Pld Acquisitions Llc Dba Av�ma Pharma Solutions. The product's dosage form is tablet and is administered via oral form.

    Is NDC 63548-0739 included in the NDC Directory?

    Yes, Indoor Outdoor Allergies with product code 63548-0739 is active and included in the NDC Directory. The product was first marketed by Pld Acquisitions Llc Dba Av�ma Pharma Solutions on July 01, 2019 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 63548-0739-3?

    The 11-digit format is 63548073903. 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 5-4-1 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
    5-4-163548-0739-35-4-263548-0739-03