Package 0363-0783-24

Brand: fexofenadine hydrochloride

Generic: fexofenadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0363-0783-24
Digits Only 0363078324
Product NDC 0363-0783
Product ID 0363-0783_99bc952b-03e9-cb28-9669-ce7dfef79b0d
Description

4 BLISTER PACK in 1 CARTON (0363-0783-24) / 6 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2020-12-14
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": "99bc952b-03e9-cb28-9669-ce7dfef79b0d", "openfda": {"unii": ["2S068B75ZU"], "spl_set_id": ["b961985e-0c18-b36f-d82e-32ff2d46fada"], "manufacturer_name": ["Walgreens Company"]}, "finished": true, "packaging": [{"sample": false, "description": "4 BLISTER PACK in 1 CARTON (0363-0783-24)  / 6 TABLET in 1 BLISTER PACK", "package_ndc": "0363-0783-24", "marketing_start_date": "20201214"}], "brand_name": "Fexofenadine hydrochloride", "product_id": "0363-0783_99bc952b-03e9-cb28-9669-ce7dfef79b0d", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "0363-0783", "generic_name": "Fexofenadine hydrochloride", "labeler_name": "Walgreens 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": "20201214", "listing_expiration_date": "20261231"}