Package 0904-6711-46

Brand: fexofenadine hydrochloride

Generic: fexofenadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0904-6711-46
Digits Only 0904671146
Product NDC 0904-6711
Description

1 BOTTLE in 1 CARTON (0904-6711-46) / 30 TABLET in 1 BOTTLE

Marketing

Marketing Status
Discontinued 2026-08-31
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": "dad01df2-a6b4-5fac-8c6a-d49c1166892f", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["0a6da401-a8a3-5d0b-f37e-c220838f7e49"], "manufacturer_name": ["MAJOR PHARMACEUTICALS"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0904-6711-46)  / 30 TABLET in 1 BOTTLE", "package_ndc": "0904-6711-46", "marketing_end_date": "20260831", "marketing_start_date": "20180427"}], "brand_name": "Fexofenadine hydrochloride", "product_id": "0904-6711_dad01df2-a6b4-5fac-8c6a-d49c1166892f", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "0904-6711", "generic_name": "Fexofenadine hydrochloride", "labeler_name": "MAJOR PHARMACEUTICALS", "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_end_date": "20260831", "marketing_start_date": "20180427"}