allergy relief
Generic: fexofenadine hydrochloride
Labeler: chain drug marketing association incDrug Facts
Product Profile
Brand Name
allergy relief
Generic Name
fexofenadine hydrochloride
Labeler
chain drug marketing association inc
Dosage Form
TABLET
Routes
Active Ingredients
fexofenadine hydrochloride 180 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
63868-334
Product ID
63868-334_24357d51-61dd-61b5-e063-6294a90a12c3
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA211075
Listing Expiration
2026-12-31
Marketing Start
2021-07-06
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63868334
Hyphenated Format
63868-334
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 hydrochloride (source: ndc)
Application Number
ANDA211075 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 180 mg/1
Packaging
- 3 BLISTER PACK in 1 CARTON (63868-334-15) / 5 TABLET in 1 BLISTER PACK
- 1 BOTTLE, PLASTIC in 1 CARTON (63868-334-30) / 30 TABLET in 1 BOTTLE, PLASTIC
- 1 BOTTLE, PLASTIC in 1 BOTTLE, PLASTIC (63868-334-45) / 45 TABLET in 1 BOTTLE, PLASTIC
Packages (3)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "24357d51-61dd-61b5-e063-6294a90a12c3", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["c5d58d74-da08-eb72-e053-2a95a90adc27"], "manufacturer_name": ["CHAIN DRUG MARKETING ASSOCIATION INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (63868-334-15) / 5 TABLET in 1 BLISTER PACK", "package_ndc": "63868-334-15", "marketing_end_date": "20261130", "marketing_start_date": "20210706"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (63868-334-30) / 30 TABLET in 1 BOTTLE, PLASTIC", "package_ndc": "63868-334-30", "marketing_end_date": "20270228", "marketing_start_date": "20210706"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOTTLE, PLASTIC (63868-334-45) / 45 TABLET in 1 BOTTLE, PLASTIC", "package_ndc": "63868-334-45", "marketing_start_date": "20210706"}], "brand_name": "Allergy Relief", "product_id": "63868-334_24357d51-61dd-61b5-e063-6294a90a12c3", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "63868-334", "generic_name": "Fexofenadine Hydrochloride", "labeler_name": "CHAIN DRUG MARKETING ASSOCIATION INC", "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_start_date": "20210706", "listing_expiration_date": "20261231"}