cvs fexofenadine hydrochloride
Generic: fexofenadine hydrochloride
Labeler: cvs pharmacyDrug Facts
Product Profile
Brand Name
cvs fexofenadine hydrochloride
Generic Name
fexofenadine hydrochloride
Labeler
cvs pharmacy
Dosage Form
TABLET
Routes
Active Ingredients
fexofenadine hydrochloride 180 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
51316-183
Product ID
51316-183_41c5bbff-5362-e7e2-e063-6294a90a5fc2
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA210137
Listing Expiration
2026-12-31
Marketing Start
2025-10-22
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
51316183
Hyphenated Format
51316-183
Supplemental Identifiers
RxCUI
UPC
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
cvs fexofenadine hydrochloride (source: ndc)
Generic Name
fexofenadine hydrochloride (source: ndc)
Application Number
ANDA210137 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 180 mg/1
Packaging
- 180 TABLET in 1 BOTTLE (51316-183-00)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "41c5bbff-5362-e7e2-e063-6294a90a5fc2", "openfda": {"upc": ["0050428000618"], "unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["3d6c7b10-ed05-bbde-e063-6294a90ae92f"], "manufacturer_name": ["CVS Pharmacy"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "180 TABLET in 1 BOTTLE (51316-183-00)", "package_ndc": "51316-183-00", "marketing_start_date": "20251022"}], "brand_name": "CVS Fexofenadine Hydrochloride", "product_id": "51316-183_41c5bbff-5362-e7e2-e063-6294a90a5fc2", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "51316-183", "generic_name": "FEXOFENADINE HYDROCHLORIDE", "labeler_name": "CVS Pharmacy", "product_type": "HUMAN OTC DRUG", "brand_name_base": "CVS Fexofenadine Hydrochloride", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA210137", "marketing_category": "ANDA", "marketing_start_date": "20251022", "listing_expiration_date": "20261231"}