NDC Package 62756-543-15 Fexofenadine Hydrochloride

View Billable Units, 11-Digit Format, RxNorm

Package Information
Other Packages
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:

62756-543-15

Package Description:

30 TABLET, FILM COATED in 1 BOTTLE

Product Code:

62756-543

Proprietary Name:

Fexofenadine Hydrochloride

Usage Information:

For 30mg:adults and children 12 years of age and overtake two 30 mg tablets with water every 12 hours; do not take more than 4 tablets in 24 hourschildren 6 to under 12 years of age take one 30 mg tablet with water every 12 hours; do not take more than 2 tablets in 24 hourschildren under 6 years of agedo not useadults 65 years of age and olderask a doctorconsumers with kidney diseaseask a doctorFor 60mg:adults and children 12 years of age and overtake one 60 mg tablet with water every 12 hours; do not take more than 2 tablets in 24 hourschildren under 12 years of age do not use adults 65 years of age and olderask a doctorconsumers with kidney diseaseask a doctorFor 180mg:adults and children 12 years of age and overtake one 180 mg tablet with water once a day; do not take more than 1 tablet in 24 hourschildren under 12 years of age do not useadults 65 years of age and olderask a doctorconsumers with kidney diseaseask a doctor

11-Digit NDC Billing Format:

62756054315

NDC to RxNorm Crosswalk:

RxCUI: 997420 - fexofenadine HCl 180 MG 24 HR Oral Tablet
RxCUI: 997420 - fexofenadine hydrochloride 180 MG Oral Tablet
RxCUI: 997488 - fexofenadine HCl 30 MG Oral Tablet
RxCUI: 997488 - fexofenadine hydrochloride 30 MG Oral Tablet
RxCUI: 997501 - fexofenadine HCl 60 MG Oral Tablet

Labeler Name:

Sun Pharmaceutical Industries, Inc.

Sample Package:

FDA Application Number:

ANDA091567

Marketing Category:

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

Start Marketing Date:

02-06-2012

End Marketing Date:

06-27-2022

Listing Expiration Date:

06-27-2022

Exclude Flag:

Code Structure:

62756 - Sun Pharmaceutical Industries, Inc.
- 62756-543 - Fexofenadine Hydrochloride
  - 62756-543-15 - 30 TABLET, FILM COATED 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.

Other Product Packages

The following packages are also available for this product:

NDC Package Code	Package Description
62756-543-16	100 TABLET, FILM COATED in 1 BOTTLE
62756-543-27	1 BLISTER PACK in 1 CARTON / 5 TABLET, FILM COATED in 1 BLISTER PACK
62756-543-28	9 BLISTER PACK in 1 CARTON / 5 TABLET, FILM COATED in 1 BLISTER PACK
62756-543-29	10 BLISTER PACK in 1 CARTON / 6 TABLET, FILM COATED in 1 BLISTER PACK
62756-543-30	15 BLISTER PACK in 1 CARTON / 6 TABLET, FILM COATED in 1 BLISTER PACK
62756-543-64	5 BLISTER PACK in 1 CARTON / 6 TABLET, FILM COATED in 1 BLISTER PACK
62756-543-66	2 BLISTER PACK in 1 CARTON / 5 TABLET, FILM COATED in 1 BLISTER PACK
62756-543-74	1 BLISTER PACK in 1 CARTON / 5 TABLET, FILM COATED in 1 BLISTER PACK
62756-543-76	10 BLISTER PACK in 1 CARTON / 6 TABLET, FILM COATED in 1 BLISTER PACK
62756-543-77	9 BLISTER PACK in 1 CARTON / 5 TABLET, FILM COATED in 1 BLISTER PACK
62756-543-78	15 BLISTER PACK in 1 CARTON / 6 TABLET, FILM COATED in 1 BLISTER PACK
62756-543-83	30 TABLET, FILM COATED in 1 BOTTLE
62756-543-88	100 TABLET, FILM COATED in 1 BOTTLE
62756-543-94	2 BLISTER PACK in 1 CARTON / 5 TABLET, FILM COATED in 1 BLISTER PACK
62756-543-95	5 BLISTER PACK in 1 CARTON / 6 TABLET, FILM COATED in 1 BLISTER PACK

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 62756-543-15?

The NDC Packaged Code 62756-543-15 is assigned to a package of 30 tablet, film coated in 1 bottle of Fexofenadine Hydrochloride, labeled by Sun Pharmaceutical Industries, Inc.. The product's dosage form is and is administered via form.

Is NDC 62756-543 included in the NDC Directory?

No, Fexofenadine Hydrochloride with product code 62756-543 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Sun Pharmaceutical Industries, Inc. on February 06, 2012 and its listing in the NDC Directory is set to expire on June 27, 2022 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 62756-543-15?

The 11-digit format is 62756054315. 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	62756-543-15	5-4-2	62756-0543-15

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