fexofenadine hcl
Generic: fexofenadine hcl
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
fexofenadine hcl
Generic Name
fexofenadine hcl
Labeler
a-s medication solutions
Dosage Form
TABLET
Routes
Active Ingredients
fexofenadine hydrochloride 180 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-6965
Product ID
50090-6965_72dc2e57-df1a-4d62-a8a2-cde96890bc2c
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA204097
Listing Expiration
2026-12-31
Marketing Start
2019-02-18
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500906965
Hyphenated Format
50090-6965
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
- 1 BOTTLE in 1 CARTON (50090-6965-0) / 30 TABLET in 1 BOTTLE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "72dc2e57-df1a-4d62-a8a2-cde96890bc2c", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["767b082e-915d-482f-8c6b-22b6e23bca19"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (50090-6965-0) / 30 TABLET in 1 BOTTLE", "package_ndc": "50090-6965-0", "marketing_start_date": "20231220"}], "brand_name": "Fexofenadine HCL", "product_id": "50090-6965_72dc2e57-df1a-4d62-a8a2-cde96890bc2c", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "50090-6965", "generic_name": "Fexofenadine HCL", "labeler_name": "A-S Medication Solutions", "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": "20190218", "listing_expiration_date": "20261231"}