Package 77771-201-05

Brand: fexofenadine hcl

Generic: fexofenadine hcl
NDC Package

Package Facts

Identity

Package NDC 77771-201-05
Digits Only 7777120105
Product NDC 77771-201
Description

500 TABLET, FILM COATED in 1 BOTTLE (77771-201-05)

Marketing

Marketing Status
Marketed Since 2025-03-10
Brand fexofenadine hcl
Generic fexofenadine hcl
Sample Package No

Linked Drug Pages (1)

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 (77771-201-01)", "package_ndc": "77771-201-01", "marketing_start_date": "20250310"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (77771-201-05)", "package_ndc": "77771-201-05", "marketing_start_date": "20250310"}], "brand_name": "fexofenadine hcl", "product_id": "77771-201_302845c7-2356-3b13-e063-6394a90a0e26", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "77771-201", "generic_name": "fexofenadine hcl", "labeler_name": "Radha Pharmaceuticals", "product_type": "HUMAN OTC DRUG", "brand_name_base": "fexofenadine hcl", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA204507", "marketing_category": "ANDA", "marketing_start_date": "20250310", "listing_expiration_date": "20261231"}