Robotablets Tablet
NDC Package 71598-015-30

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

Robotablets (dextromethorphan) tablets is only use this product according to these directions or as directed by a doctordo not exceed 4 tablets in any 24-hour periodthis adult product is not intended for use in children under 12 years of ageAgeDose adults and children 12 years and over take 1 tablet every 6 to 8 hours, as needed children under 12 years do not useOther Informationstore at 20-25°C (68-77°F).TAMPER EVIDENT: Do not use if safety seal under child-resistant cap is broken or missing. This formulation utilizes a tablet delivery system. Marketed by Dxm Pharmaceutical, Inc, this product is identified by NDC 71598-015 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
71598-015-30
Package Description
100 TABLET in 1 BOTTLE, PLASTIC
Product Code
11-Digit Billing Format
71598001530

Clinical Specifications

Proprietary Name
Robotablets
Non-Proprietary Name
Dextromethorphan
Substance Name
Dextromethorphan
Dosage Form
Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Usage Information
Only use this product according to these directions or as directed by a doctordo not exceed 4 tablets in any 24-hour periodthis adult product is not intended for use in children under 12 years of ageAgeDose adults and children 12 years and over take 1 tablet every 6 to 8 hours, as needed children under 12 years do not useOther Informationstore at 20-25°C (68-77°F).TAMPER EVIDENT: Do not use if safety seal under child-resistant cap is broken or missing.

Regulatory & Marketing

Labeler Name
Dxm Pharmaceutical, Inc
Product Type
Human Otc Drug
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
10-15-2020
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 71598-015-30 identifies a specific commercial package of 100 tablet in 1 bottle, plastic of Robotablets, a human over the counter drug labeled by Dxm Pharmaceutical, Inc. This tablet is formulated for oral use and contains dextromethorphan 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 Dxm Pharmaceutical, Inc on October 15, 2020. The current certification is valid through December 31, 2026.

How is this Dxm Pharmaceutical, Inc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 71598001530. 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)
71598-015-30
11-Digit CMS (5-4-2)
71598-0015-30

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