Propranolol Hydrochloride
NDC Package 43478-902-88

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

Package Information

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

Propranolol Hydrochloride is a . Marketed by Rouses Point Pharm, this product is identified by NDC 43478-902 and is authorized under FDA application NDA018553.

Identification & Billing

NDC Package Code
43478-902-88
Package Description
100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE
Product Code
43478-902
11-Digit Billing Format
43478090288
Billing Unit
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
Units Per Package
100 EA

Clinical Specifications

Proprietary Name
Propranolol Hydrochloride ER
Dosage Form
-

Regulatory & Marketing

Labeler Name
Rouses Point Pharm
FDA Application #
NDA018553
Marketing Category
NDA AUTHORIZED GENERIC - A product marketed as a "generic" drug under an approved New Drug Application (NDA), rather than an Abbreviated New Drug Application (ANDA),.
Start Marketing Date
02-25-2009
End Marketing Date
07-31-2019
Listing Expiration
07-31-2019
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 43478-902-88 identifies a specific commercial package of 100 capsule, extended release in 1 bottle of Propranolol Hydrochloride ER, labeled by Rouses Point Pharm. 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 Rouses Point Pharm on February 25, 2009. The current certification is valid through July 31, 2019.

How is this Rouses Point Pharm product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 43478090288. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 100 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)
43478-902-88
11-Digit CMS (5-4-2)
43478-0902-88

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