Package 41167-4121-4

Brand: allegra allergy

Generic: fexofenadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 41167-4121-4
Digits Only 4116741214
Product NDC 41167-4121
Product ID 41167-4121_e51229d3-e9e3-4295-b341-dd29d924d2d6
Description

1 BOTTLE, PLASTIC in 1 CARTON (41167-4121-4) / 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2011-03-03
Brand allegra allergy
Generic fexofenadine hydrochloride
Sample Package No

Linked Drug Pages (1)

Allegra Allergy ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "e51229d3-e9e3-4295-b341-dd29d924d2d6", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420", "997422", "997501", "997502"], "spl_set_id": ["81c1dcbb-28b3-4ad5-9f3d-9ccc16ddd173"], "manufacturer_name": ["Chattem, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (41167-4121-1)  / 60 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "41167-4121-1", "marketing_start_date": "20210601"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (41167-4121-4)  / 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "41167-4121-4", "marketing_start_date": "20110303"}], "brand_name": "Allegra Allergy", "product_id": "41167-4121_e51229d3-e9e3-4295-b341-dd29d924d2d6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "41167-4121", "generic_name": "fexofenadine hydrochloride", "labeler_name": "Chattem, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Allegra Allergy", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "NDA020872", "marketing_category": "NDA", "marketing_start_date": "20110303", "listing_expiration_date": "20271231"}