Allergy Relief

Product NDC: 37808-425
11-digit product format: 378080425
Labeler code: 37808
Product ID: 37808-425_570179ef-c32d-4afa-90cb-24966184041e
Type: HUMAN OTC DRUG
Nonproprietary name: Fexofenadine HCl
Dosage form: TABLET, FILM COATED
Route: ORAL
Labeler: H E B
Application: ANDA076447
Marketing category: ANDA
Marketing start: 2011-08-24
Marketing end: 0000-00-00
Substance: FEXOFENADINE HYDROCHLORIDE
Active strength: 60 mg/1
NDC exclude flag: No
Listing certified through: 2022-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
37808-425-53	2021-07-23	C162847	48780-1	c7ccaba7-24ab-fd44-e053-dadaa90aa01b	55af2c65-6db9-4abc-94e6-df88b99dfc60

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
37808-425-53	EA - Each	37808-425	3c4c94c7-e924-475a-9da6-8a0a699e494c	1	2022-06-06

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version	Uploaded
FEXOFENADINE HYDROCHLORIDE	ACTIVE INGREDIENT	2S068B75ZU	ALLERGY RELIEF (FEXOFENADINE HCL) TABLET, FILM COATED [H E B]	1
FEXOFENADINE	ACTIVE MOIETY	E6582LOH6V	ALLERGY RELIEF (FEXOFENADINE HCL) TABLET, FILM COATED [H E B]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
37808-425	ALLERGY RELIEF (FEXOFENADINE HCL) TABLET, FILM COATED [H E B]	5	Legacy NDC	20210724_55af2c65-6db9-4abc-94e6-df88b99dfc60.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
37808-425-53	37808042553	12 BLISTER PACK in 1 CARTON (37808-425-53) > 1 TABLET, FILM COATED in 1 BLISTER PACK	12 blister pack	2011-08-24	0000-00-00	No	No	Current