allegra allergy

Generic: fexofenadine hydrochloride

Labeler: navajo manufacturing company inc.
NDC Directory HUMAN OTC DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name allegra allergy
Generic Name fexofenadine hydrochloride
Labeler navajo manufacturing company inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

fexofenadine hydrochloride 180 mg/1

Manufacturer
Navajo Manufacturing Company Inc.

Identifiers & Regulatory

Product NDC 67751-033
Product ID 67751-033_2384a3dd-030a-f17e-e063-6394a90a90a1
Product Type HUMAN OTC DRUG
Marketing Category NDA
Application Number NDA020872
Listing Expiration 2026-12-31
Marketing Start 2015-05-12

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 67751033
Hyphenated Format 67751-033

Supplemental Identifiers

RxCUI
997420 997422
UNII
2S068B75ZU

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 allegra allergy (source: ndc)
Generic Name fexofenadine hydrochloride (source: ndc)
Application Number NDA020872 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 180 mg/1
source: ndc
Packaging
  • 1 BLISTER PACK in 1 CARTON (67751-033-02) / 1 TABLET, FILM COATED in 1 BLISTER PACK
source: ndc

Packages (1)

67751-033-02 1 BLISTER PACK in 1 CARTON (67751-033-02) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Ingredients (1)

fexofenadine hydrochloride (180 mg/1)

Linked Drug Pages (1)

Allegra Allergy ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2384a3dd-030a-f17e-e063-6394a90a90a1", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420", "997422"], "spl_set_id": ["e8a00fa1-79af-4ce6-885f-0ce12c5da836"], "manufacturer_name": ["Navajo Manufacturing Company Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (67751-033-02)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "67751-033-02", "marketing_start_date": "20160331"}], "brand_name": "Allegra Allergy", "product_id": "67751-033_2384a3dd-030a-f17e-e063-6394a90a90a1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "67751-033", "generic_name": "FEXOFENADINE HYDROCHLORIDE", "labeler_name": "Navajo Manufacturing Company Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Allegra Allergy", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "NDA020872", "marketing_category": "NDA", "marketing_start_date": "20150512", "listing_expiration_date": "20261231"}