NDC Package 83324-145-24 Daytime Cold And Flu

Acetaminophen Dextromethorphan Hbr Phenylephrine Hcl 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:
83324-145-24
Package Description:
24 BLISTER PACK in 1 CARTON / 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product Code:
Proprietary Name:
Daytime Cold And Flu
Non-Proprietary Name:
Acetaminophen Dextromethorphan Hbr Phenylephrine Hcl
Substance Name:
Acetaminophen; Dextromethorphan Hydrobromide; Phenylephrine Hydrochloride
Usage Information:
Do not take more than directed (see Overdose warning) do not take more than 4 doses in 24 hours adults and children 12 years and over: take 2 softgels with water every 4 hours swallow whole; do not crush, chew, or dissolve children under 12 years: do not use when using other Daytime or Nighttime products, carefully read each label to ensure correct dosing
11-Digit NDC Billing Format:
83324014524
Product Type:
Human Otc Drug
Labeler Name:
Quality Choice (chain Drug Marketing Association)
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:
M012
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
07-31-2024
Listing Expiration Date:
12-31-2026
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 83324-145-24?

The NDC Packaged Code 83324-145-24 is assigned to a package of 24 blister pack in 1 carton / 1 capsule, liquid filled in 1 blister pack of Daytime Cold And Flu, a human over the counter drug labeled by Quality Choice (chain Drug Marketing Association). The product's dosage form is capsule, liquid filled and is administered via oral form.

Is NDC 83324-145 included in the NDC Directory?

Yes, Daytime Cold And Flu with product code 83324-145 is active and included in the NDC Directory. The product was first marketed by Quality Choice (chain Drug Marketing Association) on July 31, 2024 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 83324-145-24?

The 11-digit format is 83324014524. 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
5-3-283324-145-245-4-283324-0145-24