fexofenadine hcl

Generic: fexofenadine hcl

Labeler: bryant ranch prepack
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name fexofenadine hcl
Generic Name fexofenadine hcl
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

fexofenadine hydrochloride 180 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-1217
Product ID 71335-1217_7921f011-b1c5-4bf9-977c-dea10b285be0
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 713351217
Hyphenated Format 71335-1217

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 (71335-1217-1)
  • 15 TABLET in 1 BOTTLE (71335-1217-2)
  • 60 TABLET in 1 BOTTLE (71335-1217-3)
  • 90 TABLET in 1 BOTTLE (71335-1217-4)
  • 5 TABLET in 1 BOTTLE (71335-1217-5)
  • 180 TABLET in 1 BOTTLE (71335-1217-6)
  • 100 TABLET in 1 BOTTLE (71335-1217-7)
source: ndc

Packages (7)

71335-1217-1 30 TABLET in 1 BOTTLE (71335-1217-1) 71335-1217-2 15 TABLET in 1 BOTTLE (71335-1217-2) 71335-1217-3 60 TABLET in 1 BOTTLE (71335-1217-3) 71335-1217-4 90 TABLET in 1 BOTTLE (71335-1217-4) 71335-1217-5 5 TABLET in 1 BOTTLE (71335-1217-5) 71335-1217-6 180 TABLET in 1 BOTTLE (71335-1217-6) 71335-1217-7 100 TABLET in 1 BOTTLE (71335-1217-7)

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": "7921f011-b1c5-4bf9-977c-dea10b285be0", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["6bc92969-0d06-4bf5-a634-80964464546c"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1217-1)", "package_ndc": "71335-1217-1", "marketing_start_date": "20190514"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (71335-1217-2)", "package_ndc": "71335-1217-2", "marketing_start_date": "20190514"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-1217-3)", "package_ndc": "71335-1217-3", "marketing_start_date": "20190514"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-1217-4)", "package_ndc": "71335-1217-4", "marketing_start_date": "20190514"}, {"sample": false, "description": "5 TABLET in 1 BOTTLE (71335-1217-5)", "package_ndc": "71335-1217-5", "marketing_start_date": "20190514"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (71335-1217-6)", "package_ndc": "71335-1217-6", "marketing_start_date": "20190514"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-1217-7)", "package_ndc": "71335-1217-7", "marketing_start_date": "20190514"}], "brand_name": "Fexofenadine HCL", "product_id": "71335-1217_7921f011-b1c5-4bf9-977c-dea10b285be0", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "71335-1217", "generic_name": "Fexofenadine HCL", "labeler_name": "Bryant Ranch Prepack", "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"}