Package 51316-183-00

Brand: cvs fexofenadine hydrochloride

Generic: fexofenadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51316-183-00
Digits Only 5131618300
Product NDC 51316-183
Description

180 TABLET in 1 BOTTLE (51316-183-00)

Marketing

Marketing Status
Marketed Since 2025-10-22
Brand cvs fexofenadine hydrochloride
Generic fexofenadine hydrochloride
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "41c5bbff-5362-e7e2-e063-6294a90a5fc2", "openfda": {"upc": ["0050428000618"], "unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["3d6c7b10-ed05-bbde-e063-6294a90ae92f"], "manufacturer_name": ["CVS Pharmacy"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "180 TABLET in 1 BOTTLE (51316-183-00)", "package_ndc": "51316-183-00", "marketing_start_date": "20251022"}], "brand_name": "CVS Fexofenadine Hydrochloride", "product_id": "51316-183_41c5bbff-5362-e7e2-e063-6294a90a5fc2", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "51316-183", "generic_name": "FEXOFENADINE HYDROCHLORIDE", "labeler_name": "CVS Pharmacy", "product_type": "HUMAN OTC DRUG", "brand_name_base": "CVS Fexofenadine Hydrochloride", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA210137", "marketing_category": "ANDA", "marketing_start_date": "20251022", "listing_expiration_date": "20261231"}