fexofenadine hydrochloride

Generic: fexofenadine hydrochloride

Labeler: 7-eleven
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name fexofenadine hydrochloride
Generic Name fexofenadine hydrochloride
Labeler 7-eleven
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

fexofenadine hydrochloride 180 mg/1

Manufacturer
7-eleven

Identifiers & Regulatory

Product NDC 10202-229
Product ID 10202-229_d5914c05-e8db-4c79-82d0-a279d1304118
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA202039
Listing Expiration 2026-12-31
Marketing Start 2015-01-15

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 10202229
Hyphenated Format 10202-229

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 fexofenadine hydrochloride (source: ndc)
Generic Name fexofenadine hydrochloride (source: ndc)
Application Number ANDA202039 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 180 mg/1
source: ndc
Packaging
  • 1 BLISTER PACK in 1 CARTON (10202-229-66) / 10 TABLET, FILM COATED in 1 BLISTER PACK
source: ndc

Packages (1)

10202-229-66 1 BLISTER PACK in 1 CARTON (10202-229-66) / 10 TABLET, FILM COATED in 1 BLISTER PACK

Ingredients (1)

fexofenadine hydrochloride (180 mg/1)

Linked Drug Pages (1)

Fexofenadine hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d5914c05-e8db-4c79-82d0-a279d1304118", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["d5914c05-e8db-4c79-82d0-a279d1304118"], "manufacturer_name": ["7-eleven"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (10202-229-66)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "10202-229-66", "marketing_start_date": "20150115"}], "brand_name": "Fexofenadine hydrochloride", "product_id": "10202-229_d5914c05-e8db-4c79-82d0-a279d1304118", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "10202-229", "generic_name": "Fexofenadine hydrochloride", "labeler_name": "7-eleven", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Fexofenadine hydrochloride", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA202039", "marketing_category": "ANDA", "marketing_start_date": "20150115", "listing_expiration_date": "20261231"}