Package 50090-1234-0

Brand: allegra allergy

Generic: fexofenadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-1234-0
Digits Only 5009012340
Product NDC 50090-1234
Product ID 50090-1234_9840fda7-e713-4573-8029-046a50c67462
Description

1 BOTTLE, PLASTIC in 1 CARTON (50090-1234-0) / 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2014-11-28
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": "9840fda7-e713-4573-8029-046a50c67462", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420", "997422", "997501", "997502"], "spl_set_id": ["b5ce28f8-f6c3-4113-9317-e1c98e5030ef"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (50090-1234-0)  / 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "50090-1234-0", "marketing_start_date": "20141128"}], "brand_name": "ALLEGRA ALLERGY", "product_id": "50090-1234_9840fda7-e713-4573-8029-046a50c67462", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "50090-1234", "generic_name": "fexofenadine hydrochloride", "labeler_name": "A-S Medication Solutions", "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": "20261231"}