allergy relief
Generic: fexofenadine hcl
Labeler: p & l development, llcDrug Facts
Product Profile
Brand Name
allergy relief
Generic Name
fexofenadine hcl
Labeler
p & l development, llc
Dosage Form
TABLET, COATED
Routes
Active Ingredients
fexofenadine hydrochloride 180 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
59726-701
Product ID
59726-701_20021f32-e254-4422-a17c-48c3b8704008
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA204507
Listing Expiration
2026-12-31
Marketing Start
2021-08-20
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
59726701
Hyphenated Format
59726-701
Supplemental Identifiers
RxCUI
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
allergy relief (source: ndc)
Generic Name
fexofenadine hcl (source: ndc)
Application Number
ANDA204507 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 180 mg/1
Packaging
- 1 BOTTLE, PLASTIC in 1 BOX (59726-701-15) / 150 TABLET, COATED in 1 BOTTLE, PLASTIC
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "20021f32-e254-4422-a17c-48c3b8704008", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["35b807b5-2e7a-446b-b378-eb5391ddfd14"], "manufacturer_name": ["P & L Development, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (59726-701-15) / 150 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "59726-701-15", "marketing_start_date": "20210820"}], "brand_name": "Allergy Relief", "product_id": "59726-701_20021f32-e254-4422-a17c-48c3b8704008", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "59726-701", "generic_name": "Fexofenadine HCl", "labeler_name": "P & L Development, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Allergy Relief", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA204507", "marketing_category": "ANDA", "marketing_start_date": "20210820", "listing_expiration_date": "20261231"}