allergy relief

Generic: fexofenadine hydrochloride

Labeler: chain drug consortium
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name allergy relief
Generic Name fexofenadine hydrochloride
Labeler chain drug consortium
Dosage Form TABLET
Routes
ORAL
Active Ingredients

fexofenadine hydrochloride 180 mg/1

Manufacturer
CHAIN DRUG CONSORTIUM

Identifiers & Regulatory

Product NDC 68016-887
Product ID 68016-887_24340f37-44e1-b094-e063-6294a90a7886
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA211075
Marketing Start 2021-07-08
Marketing End 2026-09-30

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 68016887
Hyphenated Format 68016-887

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 allergy relief (source: ndc)
Generic Name fexofenadine hydrochloride (source: ndc)
Application Number ANDA211075 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 180 mg/1
source: ndc
Packaging
  • 3 BLISTER PACK in 1 CARTON (68016-887-15) / 5 TABLET in 1 BLISTER PACK
  • 1 BOTTLE, PLASTIC in 1 CARTON (68016-887-30) / 30 TABLET in 1 BOTTLE, PLASTIC
  • 1 BOTTLE, PLASTIC in 1 CARTON (68016-887-45) / 45 TABLET in 1 BOTTLE, PLASTIC
source: ndc

Packages (3)

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": "24340f37-44e1-b094-e063-6294a90a7886", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["8eee26c2-af58-469c-b855-c3bfc8bd7e2d"], "manufacturer_name": ["CHAIN DRUG CONSORTIUM"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (68016-887-15)  / 5 TABLET in 1 BLISTER PACK", "package_ndc": "68016-887-15", "marketing_end_date": "20260930", "marketing_start_date": "20210708"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (68016-887-30)  / 30 TABLET in 1 BOTTLE, PLASTIC", "package_ndc": "68016-887-30", "marketing_end_date": "20260930", "marketing_start_date": "20210708"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (68016-887-45)  / 45 TABLET in 1 BOTTLE, PLASTIC", "package_ndc": "68016-887-45", "marketing_end_date": "20260930", "marketing_start_date": "20210708"}], "brand_name": "Allergy Relief", "product_id": "68016-887_24340f37-44e1-b094-e063-6294a90a7886", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "68016-887", "generic_name": "Fexofenadine Hydrochloride", "labeler_name": "CHAIN DRUG CONSORTIUM", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Allergy Relief", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA211075", "marketing_category": "ANDA", "marketing_end_date": "20260930", "marketing_start_date": "20210708"}