up and up non drowsy allergy relief

Generic: fexofenadine hydrochloride

Labeler: target corporation
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name up and up non drowsy allergy relief
Generic Name fexofenadine hydrochloride
Labeler target corporation
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

fexofenadine hydrochloride 180 mg/1

Manufacturer
Target Corporation

Identifiers & Regulatory

Product NDC 82442-300
Product ID 82442-300_bd226cd0-be8c-4db9-878f-5c84f6016dcc
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA212971
Listing Expiration 2026-12-31
Marketing Start 2024-03-04

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 82442300
Hyphenated Format 82442-300

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 up and up non drowsy 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
  • 1 BOTTLE in 1 CARTON (82442-300-72) / 60 TABLET, COATED in 1 BOTTLE
source: ndc

Packages (1)

Ingredients (1)

fexofenadine hydrochloride (180 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "bd226cd0-be8c-4db9-878f-5c84f6016dcc", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["d251b0a6-bc31-45b6-aaa8-f50f8336d959"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (82442-300-72)  / 60 TABLET, COATED in 1 BOTTLE", "package_ndc": "82442-300-72", "marketing_start_date": "20240304"}], "brand_name": "up and up non drowsy allergy relief", "product_id": "82442-300_bd226cd0-be8c-4db9-878f-5c84f6016dcc", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "82442-300", "generic_name": "fexofenadine hydrochloride", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "up and up non drowsy allergy relief", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA212971", "marketing_category": "ANDA", "marketing_start_date": "20240304", "listing_expiration_date": "20261231"}