Nitetime
NDC Package 33992-0621-0

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Nitetime is take only as directed - see Overdose warningdo not exceed 4 doses per 24 hrsAdults & children 12 years and over2 softgels with water every 6 hrsChildren 4 to under 12 yearsask a doctorChildren under 4 yearsdo not use. Marketed by Greenbrier International, this product is identified by NDC 33992-0621 and is authorized under FDA application part341.

Identification & Billing

NDC Package Code
33992-0621-0
Package Description
1 BLISTER PACK in 1 CARTON / 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product Code
33992-0621
11-Digit Billing Format
33992062100
RxNorm Crosswalk
  • RxCUI: 1094549 - acetaminophen 325 MG / dextromethorphan HBr 15 MG / doxylamine succinate 6.25 MG Oral Capsule
  • RxCUI: 1094549 - acetaminophen 325 MG / dextromethorphan hydrobromide 15 MG / doxylamine succinate 6.25 MG Oral Capsule
  • RxCUI: 1094549 - APAP 325 MG / dextromethorphan hydrobromide 15 MG / doxylamine succinate 6.25 MG Oral Capsule

Clinical Specifications

Proprietary Name
Nitetime Multi-symptom Cold/flu Relief
Dosage Form
-
Usage Information
Take only as directed - see Overdose warningdo not exceed 4 doses per 24 hrsAdults & children 12 years and over2 softgels with water every 6 hrsChildren 4 to under 12 yearsask a doctorChildren under 4 yearsdo not use

Regulatory & Marketing

Labeler Name
Greenbrier International
FDA Application #
part341
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
01-04-2013
Listing Expiration
12-31-2019
Exclude Flag
I
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 33992-0621-0 identifies a specific commercial package of 1 blister pack in 1 carton / 10 capsule, liquid filled in 1 blister pack of Nitetime Multi-symptom Cold/flu Relief, labeled by Greenbrier International. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Greenbrier International on January 04, 2013. The current certification is valid through December 31, 2019.

How is this Greenbrier International product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 33992062100. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-4-1)
33992-0621-0
11-Digit CMS (5-4-2)
33992-0621-00

Note: The zero is added to the Package segment to maintain the 5-4-2 structure.