allegra allergy
Generic: fexofenadine hydrochloride
Labeler: lil' drug store products, incDrug Facts
Product Profile
Brand Name
allegra allergy
Generic Name
fexofenadine hydrochloride
Labeler
lil' drug store products, inc
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
fexofenadine hydrochloride 180 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
66715-9707
Product ID
66715-9707_27498b50-3572-7eca-e063-6394a90a64cb
Product Type
HUMAN OTC DRUG
Marketing Category
NDA
Application Number
NDA020872
Listing Expiration
2026-12-31
Marketing Start
2014-09-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
667159707
Hyphenated Format
66715-9707
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 180 mg/1
Packaging
- 1 BLISTER PACK in 1 CARTON (66715-9707-1) / 1 TABLET, FILM COATED in 1 BLISTER PACK
- 2 BLISTER PACK in 1 CARTON (66715-9707-2) / 1 TABLET, FILM COATED in 1 BLISTER PACK
- 5 BLISTER PACK in 1 CARTON (66715-9707-8) / 1 TABLET, FILM COATED in 1 BLISTER PACK
Packages (3)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "27498b50-3572-7eca-e063-6394a90a64cb", "openfda": {"upc": ["0366775910181"], "unii": ["2S068B75ZU"], "rxcui": ["997420", "997422"], "spl_set_id": ["b82d993a-16ff-4037-a182-7010de8e1cdd"], "manufacturer_name": ["Lil' Drug Store Products, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (66715-9707-1) / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "66715-9707-1", "marketing_start_date": "20181101"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (66715-9707-2) / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "66715-9707-2", "marketing_start_date": "20181101"}, {"sample": false, "description": "5 BLISTER PACK in 1 CARTON (66715-9707-8) / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "66715-9707-8", "marketing_start_date": "20181101"}], "brand_name": "Allegra Allergy", "product_id": "66715-9707_27498b50-3572-7eca-e063-6394a90a64cb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "66715-9707", "generic_name": "Fexofenadine Hydrochloride", "labeler_name": "Lil' Drug Store Products, 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": "20140901", "listing_expiration_date": "20261231"}