fexofenadine hcl

Generic: fexofenadine hcl

Labeler: a-s medication solutions
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name fexofenadine hcl
Generic Name fexofenadine hcl
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

fexofenadine hydrochloride 180 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-4070
Product ID 50090-4070_eb3a6d4d-e015-4e4c-bc05-2766731c7e70
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA204097
Listing Expiration 2026-12-31
Marketing Start 2016-08-19

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 500904070
Hyphenated Format 50090-4070

Supplemental Identifiers

RxCUI
997420
UNII
2S068B75ZU

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 180 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (50090-4070-0)
  • 90 TABLET in 1 BOTTLE (50090-4070-1)
  • 100 TABLET in 1 BOTTLE (50090-4070-2)
source: ndc

Packages (3)

50090-4070-0 30 TABLET in 1 BOTTLE (50090-4070-0) 50090-4070-1 90 TABLET in 1 BOTTLE (50090-4070-1) 50090-4070-2 100 TABLET in 1 BOTTLE (50090-4070-2)

Ingredients (1)

fexofenadine hydrochloride (180 mg/1)

Linked Drug Pages (1)

Fexofenadine HCL ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "eb3a6d4d-e015-4e4c-bc05-2766731c7e70", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["b420b619-e643-43e6-9b8b-81af11fdd4ed"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-4070-0)", "package_ndc": "50090-4070-0", "marketing_start_date": "20190118"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-4070-1)", "package_ndc": "50090-4070-1", "marketing_start_date": "20190118"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (50090-4070-2)", "package_ndc": "50090-4070-2", "marketing_start_date": "20211004"}], "brand_name": "Fexofenadine HCL", "product_id": "50090-4070_eb3a6d4d-e015-4e4c-bc05-2766731c7e70", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "50090-4070", "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": "20160819", "listing_expiration_date": "20261231"}