Package 51655-854-26

Brand: fexofenadine hcl

Generic: fexofenadine hcl
NDC Package

Package Facts

Identity

Package NDC 51655-854-26
Digits Only 5165585426
Product NDC 51655-854
Description

90 TABLET in 1 BOTTLE, PLASTIC (51655-854-26)

Marketing

Marketing Status
Marketed Since 2023-02-07
Brand fexofenadine hcl
Generic fexofenadine hcl
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4973eb8e-598e-13ad-e063-6394a90a8b68", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["f7584431-11aa-8213-e053-6294a90a1585"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (51655-854-26)", "package_ndc": "51655-854-26", "marketing_start_date": "20230207"}], "brand_name": "Fexofenadine HCL", "product_id": "51655-854_4973eb8e-598e-13ad-e063-6394a90a8b68", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "51655-854", "generic_name": "Fexofenadine HCL", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Fexofenadine HCL", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA204097", "marketing_category": "ANDA", "marketing_start_date": "20230207", "listing_expiration_date": "20271231"}