allergy relief

Generic: fexofenadine hydrochloride

Labeler: h e b
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name allergy relief
Generic Name fexofenadine hydrochloride
Labeler h e b
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

fexofenadine hydrochloride 180 mg/1

Manufacturer
H E B

Identifiers & Regulatory

Product NDC 37808-847
Product ID 37808-847_5857482f-bc9f-472a-b86b-ec2e2b83f6dc
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA212971
Listing Expiration 2026-12-31
Marketing Start 2021-12-22

Pharmacologic Class

Classes
histamine h1 receptor antagonists [moa] histamine-1 receptor antagonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 37808847
Hyphenated Format 37808-847

Supplemental Identifiers

RxCUI
997420
UNII
2S068B75ZU

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name allergy relief (source: ndc)
Generic Name fexofenadine hydrochloride (source: ndc)
Application Number ANDA212971 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 180 mg/1
source: ndc
Packaging
  • 15 BLISTER PACK in 1 CARTON (37808-847-22) / 1 TABLET, FILM COATED in 1 BLISTER PACK
  • 1 BOTTLE in 1 CARTON (37808-847-39) / 30 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (37808-847-49) / 40 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (37808-847-95) / 45 TABLET, FILM COATED in 1 BOTTLE
source: ndc

Packages (4)

37808-847-22 15 BLISTER PACK in 1 CARTON (37808-847-22) / 1 TABLET, FILM COATED in 1 BLISTER PACK 37808-847-39 1 BOTTLE in 1 CARTON (37808-847-39) / 30 TABLET, FILM COATED in 1 BOTTLE 37808-847-49 1 BOTTLE in 1 CARTON (37808-847-49) / 40 TABLET, FILM COATED in 1 BOTTLE 37808-847-95 1 BOTTLE in 1 CARTON (37808-847-95) / 45 TABLET, FILM COATED in 1 BOTTLE

Ingredients (1)

fexofenadine hydrochloride (180 mg/1)

Linked Drug Pages (1)

allergy relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "5857482f-bc9f-472a-b86b-ec2e2b83f6dc", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["1930968f-6dac-463d-ab01-f5334d75cb28"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "15 BLISTER PACK in 1 CARTON (37808-847-22)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "37808-847-22", "marketing_start_date": "20211222"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (37808-847-39)  / 30 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "37808-847-39", "marketing_start_date": "20211222"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (37808-847-49)  / 40 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "37808-847-49", "marketing_start_date": "20211230"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (37808-847-95)  / 45 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "37808-847-95", "marketing_start_date": "20211222"}], "brand_name": "allergy relief", "product_id": "37808-847_5857482f-bc9f-472a-b86b-ec2e2b83f6dc", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "37808-847", "generic_name": "fexofenadine hydrochloride", "labeler_name": "H E B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "allergy relief", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA212971", "marketing_category": "ANDA", "marketing_start_date": "20211222", "listing_expiration_date": "20261231"}