Package 70677-1009-2

Brand: fexofenadine hydrochloride

Generic: fexofenadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70677-1009-2
Digits Only 7067710092
Product NDC 70677-1009
Description

1 BOTTLE in 1 CARTON (70677-1009-2) / 30 TABLET in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2023-05-05
Brand fexofenadine hydrochloride
Generic fexofenadine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1982b8ab-b306-c1f8-0490-943207d2b606", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["de438313-9790-b4ea-2d28-7a19836cf5e2"], "manufacturer_name": ["Strategic Sourcing Services, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (70677-1009-1)  / 5 TABLET in 1 BLISTER PACK", "package_ndc": "70677-1009-1", "marketing_start_date": "20230505"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (70677-1009-2)  / 30 TABLET in 1 BOTTLE", "package_ndc": "70677-1009-2", "marketing_start_date": "20230505"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (70677-1009-3)  / 70 TABLET in 1 BOTTLE", "package_ndc": "70677-1009-3", "marketing_start_date": "20230505"}], "brand_name": "Fexofenadine Hydrochloride", "product_id": "70677-1009_1982b8ab-b306-c1f8-0490-943207d2b606", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "70677-1009", "generic_name": "Fexofenadine hydrochloride", "labeler_name": "Strategic Sourcing Services, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Fexofenadine Hydrochloride", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA076502", "marketing_category": "ANDA", "marketing_start_date": "20190909", "listing_expiration_date": "20261231"}