Tramadol Hydrochloride Tablet, Film Coated
NDC Package 71610-006-72

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

Package Information

Tramadol Hydrochloride tablets are indicated for the management of pain in adults that is severe enough to require an opioid analgesic and for which alternative treatments are inadequate. This formulation utilizes a tablet, film coated delivery system. Marketed by Aphena Pharma Solutions - Tennessee, Llc, this product is identified by NDC 71610-006 and is authorized under FDA application ANDA075977.

Identification & Billing

NDC Package Code
71610-006-72
Package Description
112 TABLET, FILM COATED in 1 BOTTLE
Product Code
11-Digit Billing Format
71610000672
Billing Unit
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
Units Per Package
112 EA
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Tramadol Hydrochloride
Non-Proprietary Name
Tramadol Hydrochloride
Substance Name
Tramadol Hydrochloride
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)
Usage Information
Tramadol hydrochloride tablets are indicated for the management of pain in adults that is severe enough to require an opioid analgesic and for which alternative treatments are inadequate.
DEA Schedule
Schedule IV (CIV) Substances

Regulatory & Marketing

Labeler Name
Aphena Pharma Solutions - Tennessee, Llc
Product Type
Human Prescription Drug
FDA Application #
ANDA075977
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
08-24-2017
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (71610-006). Click a package code to view its specific billing and regulatory data.

15 TABLET, FILM COATED in 1 BOTTLE
20 TABLET, FILM COATED in 1 BOTTLE
224 TABLET, FILM COATED in 1 BOTTLE
28 TABLET, FILM COATED in 1 BOTTLE
30 TABLET, FILM COATED in 1 BOTTLE
40 TABLET, FILM COATED in 1 BOTTLE
45 TABLET, FILM COATED in 1 BOTTLE
56 TABLET, FILM COATED in 1 BOTTLE
480 TABLET, FILM COATED in 1 BOTTLE
50 TABLET, FILM COATED in 1 BOTTLE
60 TABLET, FILM COATED in 1 BOTTLE
84 TABLET, FILM COATED in 1 BOTTLE
80 TABLET, FILM COATED in 1 BOTTLE
90 TABLET, FILM COATED in 1 BOTTLE
100 TABLET, FILM COATED in 1 BOTTLE
168 TABLET, FILM COATED in 1 BOTTLE
120 TABLET, FILM COATED in 1 BOTTLE
135 TABLET, FILM COATED in 1 BOTTLE
150 TABLET, FILM COATED in 1 BOTTLE
180 TABLET, FILM COATED in 1 BOTTLE
200 TABLET, FILM COATED in 1 BOTTLE
720 TABLET, FILM COATED in 1 BOTTLE
240 TABLET, FILM COATED in 1 BOTTLE
270 TABLET, FILM COATED in 1 BOTTLE
360 TABLET, FILM COATED in 1 BOTTLE
540 TABLET, FILM COATED in 1 BOTTLE

* 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 71610-006-72 identifies a specific commercial package of 112 tablet, film coated in 1 bottle of Tramadol Hydrochloride, a human prescription drug labeled by Aphena Pharma Solutions - Tennessee, Llc. This product is billed for "EA" each discreet unit and contains an estimated amount of 112 billable units per package. This tablet, film coated is formulated for oral use and contains tramadol hydrochloride 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 Aphena Pharma Solutions - Tennessee, Llc on August 24, 2017. The current certification is valid through December 31, 2026.

How is this Aphena Pharma Solutions - Tennessee, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 71610000672. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 112 total billable units per package. 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)
71610-006-72
11-Digit CMS (5-4-2)
71610-0006-72

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