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  5. NDC Package Code: 0135-1329-01 Flonase Nighttime Allergy Relief

NDC Package 0135-1329-01 Flonase Nighttime Allergy Relief

Triprolidine Hcl Tablet 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:
0135-1329-01
Package Description:
1 BLISTER PACK in 1 CARTON / 36 TABLET in 1 BLISTER PACK
Product Code:
0135-1329
Proprietary Name:
Flonase Nighttime Allergy Relief
Non-Proprietary Name:
Triprolidine Hcl
Substance Name:
Triprolidine Hydrochloride
Usage Information:
•do not use more than directed•adults and children 12 years of age and over: 1 tablet (2.5 mg) every 4 to 6 hours; not to exceed 4 tablets (10 mg) in 24 hours or as directed by a doctor•children under 12 years of age: do not use
11-Digit NDC Billing Format:
00135132901
Product Type:
Human Otc Drug
Labeler Name:
Haleon Us Holdings Llc
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):
  • TRIPROLIDINE HYDROCHLORIDE 2.5 mg/1
    • Sample Package:
    No
    FDA Application Number:
    M012
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    12-15-2022
    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.

    Frequently Asked Questions

    What is NDC 0135-1329-01?

    The NDC Packaged Code 0135-1329-01 is assigned to a package of 1 blister pack in 1 carton / 36 tablet in 1 blister pack of Flonase Nighttime Allergy Relief, a human over the counter drug labeled by Haleon Us Holdings Llc. The product's dosage form is tablet and is administered via oral form.

    Is NDC 0135-1329 included in the NDC Directory?

    Yes, Flonase Nighttime Allergy Relief with product code 0135-1329 is active and included in the NDC Directory. The product was first marketed by Haleon Us Holdings Llc on December 15, 2022 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 0135-1329-01?

    The 11-digit format is 00135132901. 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 4-4-2 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
    4-4-20135-1329-015-4-200135-1329-01