Effexor
NDC Package 21695-047-45

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

Package Information

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

Effexor is hypersensitivity to venlafaxine hydrochloride or to any excipients in the formulation. Marketed by Rebel Distributors Corp, this product is identified by NDC 21695-047 and is authorized under FDA application NDA020699.

Identification & Billing

NDC Package Code
21695-047-45
Package Description
45 CAPSULE, EXTENDED RELEASE in 1 BOTTLE
Product Code
11-Digit Billing Format
21695004745
Billing Unit
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
Units Per Package
45 EA
RxNorm Crosswalk
  • RxCUI: 313581 - venlafaxine HCl 150 MG 24HR Extended Release Oral Capsule
  • RxCUI: 313581 - 24 HR venlafaxine 150 MG Extended Release Oral Capsule
  • RxCUI: 313581 - venlafaxine (as venlafaxine HCl) 150 MG 24 HR Extended Release Oral Capsule
  • RxCUI: 313583 - venlafaxine HCl 37.5 MG 24HR Extended Release Oral Capsule
  • RxCUI: 313583 - 24 HR venlafaxine 37.5 MG Extended Release Oral Capsule

Clinical Specifications

Proprietary Name
Effexor Xr Extended-release
Dosage Form
-
Usage Information
Hypersensitivity to venlafaxine hydrochloride or to any excipients in the formulation. Concomitant use in patients taking monoamine oxidase inhibitors (MAOIs) is contraindicated (see WARNINGS).

Regulatory & Marketing

Labeler Name
Rebel Distributors Corp
FDA Application #
NDA020699
Marketing Category
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date
11-01-1997
Listing Expiration
12-31-2017
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (21695-047). Click a package code to view its specific billing and regulatory data.

15 CAPSULE, EXTENDED RELEASE 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 21695-047-45 identifies a specific commercial package of 45 capsule, extended release in 1 bottle of Effexor Xr Extended-release, labeled by Rebel Distributors Corp. This product is billed for "EA" each discreet unit and contains an estimated amount of 45 billable units per package. 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 Rebel Distributors Corp on November 01, 1997. The current certification is valid through December 31, 2017.

How is this Rebel Distributors Corp product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 21695004745. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 45 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)
21695-047-45
11-Digit CMS (5-4-2)
21695-0047-45

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