Ibuprofen And Pseudoephedrine Hydrochloride
NDC Package 51660-493-41

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.

Ibuprofen And Pseudoephedrine Hydrochloride is •do not take more than directed•the smallest effective dose should be used•adults and children 12 years of age and over:•take 1 caplet every 4 to 6 hours while symptoms persist. Marketed by Ohm Laboratories Inc., this product is identified by NDC 51660-493 and is authorized under FDA application ANDA074567.

Identification & Billing

NDC Package Code
51660-493-41
Package Description
40 TABLET, SUGAR COATED in 1 BLISTER PACK
Product Code
51660-493
11-Digit Billing Format
51660049341
Billing Unit
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
Units Per Package
40 EA

Clinical Specifications

Proprietary Name
Ibuprofen And Pseudoephedrine Hydrochloride
Dosage Form
-
Usage Information
•do not take more than directed•the smallest effective dose should be used•adults and children 12 years of age and over:•take 1 caplet every 4 to 6 hours while symptoms persist. If symptoms do not respond to 1 caplet, 2 caplets may be used.•do not use more than 6 caplets in any 24-hour period unless directed by a doctor•children under 12 years of age: do not use

Regulatory & Marketing

Labeler Name
Ohm Laboratories Inc.
FDA Application #
ANDA074567
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
10-13-2001
End Marketing Date
09-30-2025
Listing Expiration
09-30-2025
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 51660-493-41 identifies a specific commercial package of 40 tablet, sugar coated in 1 blister pack of Ibuprofen And Pseudoephedrine Hydrochloride, labeled by Ohm Laboratories Inc.. This product is billed for "EA" each discreet unit and contains an estimated amount of 40 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 Ohm Laboratories Inc. on October 13, 2001. The current certification is valid through September 30, 2025.

How is this Ohm Laboratories Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 51660049341. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 40 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)
51660-493-41
11-Digit CMS (5-4-2)
51660-0493-41

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