Package 67751-033-02

Brand: allegra allergy

Generic: fexofenadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67751-033-02
Digits Only 6775103302
Product NDC 67751-033
Product ID 67751-033_2384a3dd-030a-f17e-e063-6394a90a90a1
Description

1 BLISTER PACK in 1 CARTON (67751-033-02) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2016-03-31
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": "2384a3dd-030a-f17e-e063-6394a90a90a1", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420", "997422"], "spl_set_id": ["e8a00fa1-79af-4ce6-885f-0ce12c5da836"], "manufacturer_name": ["Navajo Manufacturing Company Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (67751-033-02)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "67751-033-02", "marketing_start_date": "20160331"}], "brand_name": "Allegra Allergy", "product_id": "67751-033_2384a3dd-030a-f17e-e063-6394a90a90a1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "67751-033", "generic_name": "FEXOFENADINE HYDROCHLORIDE", "labeler_name": "Navajo Manufacturing Company 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": "20150512", "listing_expiration_date": "20261231"}