Package 68210-2210-1

Brand: fexofenadine hydrochloride

Generic: fexofenadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68210-2210-1
Digits Only 6821022101
Product NDC 68210-2210
Product ID 68210-2210_292e71ee-f44d-0821-e063-6394a90a4187
Description

100 TABLET, FILM COATED in 1 PACKAGE (68210-2210-1)

Marketing

Marketing Status
Marketed Since 2020-03-17
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": "292e71ee-f44d-0821-e063-6394a90a4187", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["ae0f16f6-d07a-47e1-adb8-07803c6cfb13"], "manufacturer_name": ["SPIRIT PHARMACEUTICALS LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 PACKAGE (68210-2210-1)", "package_ndc": "68210-2210-1", "marketing_start_date": "20200317"}], "brand_name": "Fexofenadine Hydrochloride", "product_id": "68210-2210_292e71ee-f44d-0821-e063-6394a90a4187", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "68210-2210", "generic_name": "Fexofenadine Hydrochloride", "labeler_name": "SPIRIT PHARMACEUTICALS LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Fexofenadine Hydrochloride", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA204507", "marketing_category": "ANDA", "marketing_start_date": "20200317", "listing_expiration_date": "20261231"}