Package 11822-7663-4

Brand: fexofenadine hcl

Generic: fexofenadine hcl
NDC Package

Package Facts

Identity

Package NDC 11822-7663-4
Digits Only 1182276634
Product NDC 11822-7663
Description

70 TABLET in 1 BOTTLE (11822-7663-4)

Marketing

Marketing Status
Marketed Since 2024-10-25
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": "46553a37-c7d7-ba5b-e063-6394a90a584c", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["1ddad045-7706-ea7e-e063-6394a90a2a5a"], "manufacturer_name": ["Rite Aid"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "70 TABLET in 1 BOTTLE (11822-7663-4)", "package_ndc": "11822-7663-4", "marketing_start_date": "20241025"}], "brand_name": "Fexofenadine HCl", "product_id": "11822-7663_46553a37-c7d7-ba5b-e063-6394a90a584c", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "11822-7663", "generic_name": "Fexofenadine HCl", "labeler_name": "Rite Aid", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Fexofenadine HCl", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA211075", "marketing_category": "ANDA", "marketing_start_date": "20241025", "listing_expiration_date": "20271231"}