NDC Package 58602-717-30 Diphenhydramine Hcl And Ibuprofen

Capsule, Liquid Filled 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:
58602-717-30
Package Description:
160 CAPSULE, LIQUID FILLED in 1 BOTTLE
Product Code:
Proprietary Name:
Diphenhydramine Hcl And Ibuprofen
Non-Proprietary Name:
Diphenhydramine Hcl And Ibuprofen
Substance Name:
Diphenhydramine Hydrochloride; Ibuprofen
Usage Information:
Do not take more than directedadults and children 12 years and over: take 2 capsules at bedtimedo not take more than 2 capsules in 24 hoursOther informationeach capsule contains: potassium 20 mgread all warnings and directions before use.store at 20° to 25°C (68° to 77°F)avoid excessive heat above 40°C (104°F)protect from lightOrganic Impurities Test is PendingMeets USP dissolution test 2
11-Digit NDC Billing Format:
58602071730
NDC to RxNorm Crosswalk:
  • RxCUI: 901814 - ibuprofen 200 MG / diphenhydrAMINE HCl 25 MG Oral Capsule
  • RxCUI: 901814 - diphenhydramine hydrochloride 25 MG / ibuprofen 200 MG Oral Capsule
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Aurohealth Llc
    Dosage Form:
    Capsule, Liquid Filled - A solid dosage form in which the drug is enclosed within a soluble, gelatin shell which is plasticized by the addition of a polyol, such as sorbitol or glycerin, and is therefore of a somewhat thicker consistency than that of a hard shell capsule; typically, the active ingredients are dissolved or suspended in a liquid vehicle.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    FDA Application Number:
    ANDA210676
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    12-09-2022
    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 58602-717-30?

    The NDC Packaged Code 58602-717-30 is assigned to a package of 160 capsule, liquid filled in 1 bottle of Diphenhydramine Hcl And Ibuprofen, a human over the counter drug labeled by Aurohealth Llc. The product's dosage form is capsule, liquid filled and is administered via oral form.

    Is NDC 58602-717 included in the NDC Directory?

    Yes, Diphenhydramine Hcl And Ibuprofen with product code 58602-717 is active and included in the NDC Directory. The product was first marketed by Aurohealth Llc on December 09, 2022 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 58602-717-30?

    The 11-digit format is 58602071730. 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
    5-3-258602-717-305-4-258602-0717-30