Ibuprofen And Diphenhydramine Citrate Tablet
NDC Package 55111-565-92

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

Package Information

Ibuprofen And Diphenhydramine Citrate tablets is do not take more than directeddo not take longer than 10 days, unless directed by a doctor (see WARNINGS)adults and children 12 years and over: take 2 caplets at bedtime.do not take more than 2 caplets in 24 hours. This formulation utilizes a tablet delivery system. Marketed by Dr. Reddy's Laboratories Limited, this product is identified by NDC 55111-565 and is authorized under FDA application ANDA090619.

Identification & Billing

NDC Package Code
55111-565-92
Package Description
2500 TABLET in 1 POUCH
Product Code
55111-565
11-Digit Billing Format
55111056592
RxNorm Crosswalk
  • RxCUI: 895664 - ibuprofen 200 MG / diphenhydrAMINE citrate 38 MG Oral Tablet
  • RxCUI: 895664 - diphenhydramine citrate 38 MG / ibuprofen 200 MG Oral Tablet

Clinical Specifications

Proprietary Name
Ibuprofen And Diphenhydramine Citrate
Non-Proprietary Name
Ibuprofen And Diphenhydramine Citrate
Substance Name
Diphenhydramine Citrate; Ibuprofen
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)
Pharmacologic Class
Usage Information
Do not take more than directeddo not take longer than 10 days, unless directed by a doctor (see WARNINGS)adults and children 12 years and over: take 2 caplets at bedtime.do not take more than 2 caplets in 24 hours

Regulatory & Marketing

Labeler Name
Dr. Reddy's Laboratories Limited
Product Type
Human Otc Drug
FDA Application #
ANDA090619
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
01-31-2010
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 (55111-565). Click a package code to view its specific billing and regulatory data.

55111-565-05
1 BOTTLE in 1 CARTON / 500 TABLET in 1 BOTTLE
55111-565-14
1 BOTTLE in 1 CARTON / 20 TABLET in 1 BOTTLE
55111-565-18
1 BOTTLE in 1 CARTON / 180 TABLET in 1 BOTTLE
55111-565-30
1 BOTTLE in 1 CARTON / 30 TABLET in 1 BOTTLE
55111-565-40
1 BOTTLE in 1 CARTON / 40 TABLET in 1 BOTTLE
55111-565-80
1 BOTTLE in 1 CARTON / 80 TABLET in 1 BOTTLE
55111-565-90
1 BOTTLE in 1 CARTON / 90 TABLET 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 55111-565-92 identifies a specific commercial package of 2500 tablet in 1 pouch of Ibuprofen And Diphenhydramine Citrate, a human over the counter drug labeled by Dr. Reddy's Laboratories Limited. This tablet is formulated for oral use and contains diphenhydramine citrate; ibuprofen 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 Dr. Reddy's Laboratories Limited on January 31, 2010. The current certification is valid through December 31, 2026.

How is this Dr. Reddy's Laboratories Limited product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 55111056592. 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)
55111-565-92
11-Digit CMS (5-4-2)
55111-0565-92

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