Package 30142-091-12

Brand: fexofenadine hydrochloride

Generic: fexofenadine hydrochloride 60 mg
NDC Package

Package Facts

Identity

Package NDC 30142-091-12
Digits Only 3014209112
Product NDC 30142-091
Product ID 30142-091_31573c90-831d-5cae-0ff1-62ffa650de02
Description

2 BLISTER PACK in 1 CARTON (30142-091-12) / 6 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2022-01-03
Brand fexofenadine hydrochloride
Generic fexofenadine hydrochloride 60 mg
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": "31573c90-831d-5cae-0ff1-62ffa650de02", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997501"], "spl_set_id": ["98768939-d3d2-b294-4a20-57eba65880ab"], "manufacturer_name": ["Kroger Company"]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (30142-091-12)  / 6 TABLET in 1 BLISTER PACK", "package_ndc": "30142-091-12", "marketing_start_date": "20220103"}], "brand_name": "Fexofenadine Hydrochloride", "product_id": "30142-091_31573c90-831d-5cae-0ff1-62ffa650de02", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "30142-091", "generic_name": "Fexofenadine Hydrochloride 60 mg", "labeler_name": "Kroger Company", "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": "20220103", "listing_expiration_date": "20261231"}