Nighttime Cold And Flu
NDC Package 81660-777-01

11-digit billing NDC: 81660077701

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

Nighttime Cold And Flu is directionstake only as directed only use the dose cup provided do not exceed 4 doses per 24 hrs adults & children 12 yrs & over30 mL every 6 hrschildren 4 to under 12 yrsask a doctorchildren under 4 yrsdo not use. Marketed by Grimann, S.a. De C.v., this product is identified by NDC 81660-777 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
81660-777-01
Package Description
30 mL in 1 BOTTLE, PLASTIC
Product Code
11-Digit Billing Format
81660077701
RxNorm Crosswalk
  • RxCUI: 1043400 - acetaminophen 650 MG / dextromethorphan HBr 30 MG / doxylamine succinate 12.5 MG in 30 mL Oral Solution
  • RxCUI: 1043400 - acetaminophen 21.7 MG/ML / dextromethorphan hydrobromide 1 MG/ML / doxylamine succinate 0.417 MG/ML Oral Solution
  • RxCUI: 1043400 - acetaminophen 325 MG / dextromethorphan HBr 15 MG / doxylamine succinate 6.25 MG per 15 ML Oral Solution
  • RxCUI: 1043400 - acetaminophen 650 MG / dextromethorphan HBr 30 MG / doxylamine succinate 12.5 MG per 30 ML Oral Solution
  • RxCUI: 1043400 - APAP 21.7 MG/ML / Dextromethorphan Hydrobromide 1 MG/ML / doxylamine succinate 0.417 MG/ML Oral Solution

Clinical Specifications

Proprietary Name
Nighttime Cold And Flu
Dosage Form
-
Usage Information
Directionstake only as directed only use the dose cup provided do not exceed 4 doses per 24 hrs adults & children 12 yrs & over30 mL every 6 hrschildren 4 to under 12 yrsask a doctorchildren under 4 yrsdo not use

Regulatory & Marketing

Labeler Name
Grimann, S.a. De C.v.
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
04-11-2023
End Marketing Date
10-08-2026
Listing Expiration
10-08-2026
Exclude Flag
D
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 81660-777-01 identifies a specific commercial package of 30 ml in 1 bottle, plastic of Nighttime Cold And Flu, labeled by Grimann, S.a. De C.v.. 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 Grimann, S.a. De C.v. on April 11, 2023. The current certification is valid through October 08, 2026.

How is this Grimann, S.a. De C.v. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 81660077701. 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 (5-3-2)
81660-777-01
11-Digit CMS (5-4-2)
81660-0777-01

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