Package 10202-229-66

Brand: fexofenadine hydrochloride

Generic: fexofenadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 10202-229-66
Digits Only 1020222966
Product NDC 10202-229
Product ID 10202-229_d5914c05-e8db-4c79-82d0-a279d1304118
Description

1 BLISTER PACK in 1 CARTON (10202-229-66) / 10 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2015-01-15
Brand fexofenadine hydrochloride
Generic fexofenadine hydrochloride
Sample Package No

Linked Drug Pages (1)

Fexofenadine hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d5914c05-e8db-4c79-82d0-a279d1304118", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["d5914c05-e8db-4c79-82d0-a279d1304118"], "manufacturer_name": ["7-eleven"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (10202-229-66)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "10202-229-66", "marketing_start_date": "20150115"}], "brand_name": "Fexofenadine hydrochloride", "product_id": "10202-229_d5914c05-e8db-4c79-82d0-a279d1304118", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "10202-229", "generic_name": "Fexofenadine hydrochloride", "labeler_name": "7-eleven", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Fexofenadine hydrochloride", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA202039", "marketing_category": "ANDA", "marketing_start_date": "20150115", "listing_expiration_date": "20261231"}