fexofenadine hcl

Generic: fexofenadine hcl

Labeler: radha pharmaceuticals
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name fexofenadine hcl
Generic Name fexofenadine hcl
Labeler radha pharmaceuticals
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

fexofenadine hydrochloride 180 mg/1

Manufacturer
Radha Pharmaceuticals

Identifiers & Regulatory

Product NDC 77771-202
Product ID 77771-202_302845c7-2356-3b13-e063-6394a90a0e26
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA204507
Listing Expiration 2026-12-31
Marketing Start 2025-03-10

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 77771202
Hyphenated Format 77771-202

Supplemental Identifiers

RxCUI
997420 997501
UPC
0377771202309 0377771202057 0377771202019 0377771201012
UNII
2S068B75ZU

Packaging Origin

Original Packager
true

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 ANDA204507 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 180 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (77771-202-01)
  • 500 TABLET, FILM COATED in 1 BOTTLE (77771-202-05)
  • 30 TABLET, FILM COATED in 1 BOTTLE (77771-202-30)
source: ndc

Packages (3)

77771-202-01 100 TABLET, FILM COATED in 1 BOTTLE (77771-202-01) 77771-202-05 500 TABLET, FILM COATED in 1 BOTTLE (77771-202-05) 77771-202-30 30 TABLET, FILM COATED in 1 BOTTLE (77771-202-30)

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": "302845c7-2356-3b13-e063-6394a90a0e26", "openfda": {"upc": ["0377771202309", "0377771202057", "0377771202019", "0377771201012"], "unii": ["2S068B75ZU"], "rxcui": ["997420", "997501"], "spl_set_id": ["30283df1-6394-3a91-e063-6394a90a6776"], "manufacturer_name": ["Radha Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (77771-202-01)", "package_ndc": "77771-202-01", "marketing_start_date": "20250310"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (77771-202-05)", "package_ndc": "77771-202-05", "marketing_start_date": "20250310"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (77771-202-30)", "package_ndc": "77771-202-30", "marketing_start_date": "20250310"}], "brand_name": "fexofenadine hcl", "product_id": "77771-202_302845c7-2356-3b13-e063-6394a90a0e26", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "77771-202", "generic_name": "fexofenadine hcl", "labeler_name": "Radha Pharmaceuticals", "product_type": "HUMAN OTC DRUG", "brand_name_base": "fexofenadine hcl", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA204507", "marketing_category": "ANDA", "marketing_start_date": "20250310", "listing_expiration_date": "20261231"}