Alert Tablet, Film Coated
NDC Package 49483-343-44

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

Package Information

Alert (caffeine) tablets is useshelps restore mental alertness or wakefulness when experiencing fatigue or drowsiness. This formulation utilizes a tablet, film coated delivery system. Marketed by Time Cap Labs, Inc, this product is identified by NDC 49483-343 and is authorized under FDA application part340.

Identification & Billing

NDC Package Code
49483-343-44
Package Description
40 TABLET, FILM COATED in 1 BOTTLE
Product Code
49483-343
11-Digit Billing Format
49483034344
RxNorm Crosswalk
RxCUI: 198520 - caffeine 200 MG Oral Tablet

Clinical Specifications

Proprietary Name
Alert
Non-Proprietary Name
Caffeine
Substance Name
Caffeine
Dosage Form
Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
CAFFEINE 200 mg/1
Pharmacologic Class
Usage Information
Useshelps restore mental alertness or wakefulness when experiencing fatigue or drowsiness

Regulatory & Marketing

Labeler Name
Time Cap Labs, Inc
Product Type
Human Otc Drug
FDA Application #
part340
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
11-30-2011
Listing Expiration
12-31-2026
Exclude Flag
N
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 49483-343-44 identifies a specific commercial package of 40 tablet, film coated in 1 bottle of Alert, a human over the counter drug labeled by Time Cap Labs, Inc. This tablet, film coated is formulated for oral use and contains caffeine as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Time Cap Labs, Inc on November 30, 2011. The current certification is valid through December 31, 2026.

How is this Time Cap Labs, Inc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 49483034344. 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)
49483-343-44
11-Digit CMS (5-4-2)
49483-0343-44

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