Package 68001-439-00

Brand: fexofenadine hydrochloride

Generic: fexofenadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68001-439-00
Digits Only 6800143900
Product NDC 68001-439
Product ID 68001-439_bd31cd71-9281-7667-e053-2995a90a4ac0
Description

1 BOTTLE in 1 CARTON (68001-439-00) / 100 TABLET in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2020-06-19
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": "bd31cd71-9281-7667-e053-2995a90a4ac0", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420", "997501"], "spl_set_id": ["a86aebd0-937e-5d73-e053-2995a90a656a"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (68001-439-00)  / 100 TABLET in 1 BOTTLE", "package_ndc": "68001-439-00", "marketing_start_date": "20200619"}], "brand_name": "Fexofenadine hydrochloride", "product_id": "68001-439_bd31cd71-9281-7667-e053-2995a90a4ac0", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "68001-439", "generic_name": "Fexofenadine hydrochloride", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Fexofenadine hydrochloride", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA076502", "marketing_category": "ANDA", "marketing_start_date": "20200619", "listing_expiration_date": "20261231"}