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62756-545 NDC - FEXOFENADINE HYDROCHLORIDE ()

Drug Information

Product NDC: 62756-545

Proprietary Name: FEXOFENADINE HYDROCHLORIDE

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Pharmacy Class(es):
  • Histamine H1 Receptor Antagonists [MoA];
  • Histamine-1 Receptor Antagonist [EPC]

Labeler Information

Labeler Name: Sun Pharmaceutical Industries, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:2/6/2012

Package Information

No. Package Code Package Description Billing Unit
162756-545-1530 TABLET, FILM COATED in 1 BOTTLE (62756-545-15)
262756-545-1745 TABLET, FILM COATED in 1 BOTTLE (62756-545-17)
362756-545-1870 TABLET, FILM COATED in 1 BOTTLE (62756-545-18)
462756-545-1990 TABLET, FILM COATED in 1 BOTTLE (62756-545-19)
562756-545-20150 TABLET, FILM COATED in 1 BOTTLE (62756-545-20)
662756-545-21180 TABLET, FILM COATED in 1 BOTTLE (62756-545-21)
762756-545-22300 TABLET, FILM COATED in 1 BOTTLE (62756-545-22)
862756-545-253 BLISTER PACK in 1 CARTON (62756-545-25) / 5 TABLET, FILM COATED in 1 BLISTER PACK (62756-545-31)
962756-545-271 BLISTER PACK in 1 CARTON (62756-545-27) / 5 TABLET, FILM COATED in 1 BLISTER PACK (62756-545-31)
1062756-545-645 BLISTER PACK in 1 CARTON (62756-545-64) / 6 TABLET, FILM COATED in 1 BLISTER PACK
1162756-545-662 BLISTER PACK in 1 CARTON (62756-545-66) / 5 TABLET, FILM COATED in 1 BLISTER PACK
1262756-545-741 BLISTER PACK in 1 CARTON (62756-545-74) / 5 TABLET, FILM COATED in 1 BLISTER PACK
1362756-545-7610 BLISTER PACK in 1 CARTON (62756-545-76) / 6 TABLET, FILM COATED in 1 BLISTER PACK
1462756-545-779 BLISTER PACK in 1 CARTON (62756-545-77) / 5 TABLET, FILM COATED in 1 BLISTER PACK
1562756-545-7815 BLISTER PACK in 1 CARTON (62756-545-78) / 6 TABLET, FILM COATED in 1 BLISTER PACK
1662756-545-8330 TABLET, FILM COATED in 1 BOTTLE (62756-545-83)
1762756-545-88100 TABLET, FILM COATED in 1 BOTTLE (62756-545-88)
1862756-545-942 BLISTER PACK in 1 CARTON (62756-545-94) / 5 TABLET, FILM COATED in 1 BLISTER PACK (62756-545-31)

NDC Record

Field Name Field Value Definition
PRODUCT NDC62756-545The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMEFEXOFENADINE HYDROCHLORIDEThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE2/6/2012This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMESun Pharmaceutical Industries, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
PRODUCT NDC62756-545The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMEFEXOFENADINE HYDROCHLORIDEThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE6/30/2022This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMESun Pharmaceutical Industries, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023
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