fexofenadine hcl
Generic: fexofenadine hcl
Labeler: northwind health company, llcDrug Facts
Product Profile
Brand Name
fexofenadine hcl
Generic Name
fexofenadine hcl
Labeler
northwind health company, llc
Dosage Form
TABLET
Routes
Active Ingredients
fexofenadine hydrochloride 180 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
51655-854
Product ID
51655-854_4973eb8e-598e-13ad-e063-6394a90a8b68
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA204097
Listing Expiration
2027-12-31
Marketing Start
2023-02-07
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
51655854
Hyphenated Format
51655-854
Supplemental Identifiers
RxCUI
UNII
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 hcl (source: ndc)
Generic Name
fexofenadine hcl (source: ndc)
Application Number
ANDA204097 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 180 mg/1
Packaging
- 90 TABLET in 1 BOTTLE, PLASTIC (51655-854-26)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4973eb8e-598e-13ad-e063-6394a90a8b68", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["f7584431-11aa-8213-e053-6294a90a1585"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (51655-854-26)", "package_ndc": "51655-854-26", "marketing_start_date": "20230207"}], "brand_name": "Fexofenadine HCL", "product_id": "51655-854_4973eb8e-598e-13ad-e063-6394a90a8b68", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "51655-854", "generic_name": "Fexofenadine HCL", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Fexofenadine HCL", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA204097", "marketing_category": "ANDA", "marketing_start_date": "20230207", "listing_expiration_date": "20271231"}