NDC Package 37808-897-26 Rx Act Ibuprofen Childrens

View Billable Units, 11-Digit Format, RxNorm

Package Information
Frequently Asked Questions

Package Information

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

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:

37808-897-26

Package Description:

1 BOTTLE in 1 CARTON / 120 mL in 1 BOTTLE

Product Code:

37808-897

Proprietary Name:

Rx Act Ibuprofen Childrens

Usage Information:

•this product does not contain directions or complete warnings for adult use •do not give more than directed •shake well before using •find right dose on chart. If possible, use weight to dose; otherwise use age. •use only enclosed measuring cup •if needed, repeat dose every 6-8 hours •do not use more than 4 times a day •replace original bottle cap to maintain child resistance •wash dosage cup after each use Dosing ChartWeight (lbs)Age(yrs)Dose (teaspoonful or mL)under 2 yearsask a doctor24-35 lbs2-3 years1 tsp or 5 mL36-47 lbs4-5 years1 ½ tsp or 7.5 mL48-59 lbs6-8 years2 tsp or 10 mL60-71 lbs9-10 years2 ½ tsp or 12.5 mL72-95 lbs11 years3 tsp or 15 mL

11-Digit NDC Billing Format:

37808089726

Billing Unit:

ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.

Labeler Name:

H E B

Sample Package:

FDA Application Number:

ANDA074937

Marketing Category:

ANDA - A product marketed under an approved Abbreviated New Drug Application.

Start Marketing Date:

01-06-1999

End Marketing Date:

07-08-2013

Listing Expiration Date:

07-08-2013

Exclude Flag:

Code Structure:

37808 - H E B
- 37808-897 - Rx Act Ibuprofen
  - 37808-897-26 - 1 BOTTLE in 1 CARTON / 120 mL in 1 BOTTLE

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 disclaimer below.

Frequently Asked Questions

What is NDC 37808-897-26?

The NDC Packaged Code 37808-897-26 is assigned to a package of 1 bottle in 1 carton / 120 ml in 1 bottle of Rx Act Ibuprofen Childrens, labeled by H E B. The product's dosage form is and is administered via form.

Is NDC 37808-897 included in the NDC Directory?

No, Rx Act Ibuprofen Childrens with product code 37808-897 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by H E B on January 06, 1999 and its listing in the NDC Directory is set to expire on July 08, 2013 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 37808-897-26?

The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

What is the 11-digit format for NDC 37808-897-26?

The 11-digit format is 37808089726. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-3-2	37808-897-26	5-4-2	37808-0897-26

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