Package 21130-405-30

Brand: iallergy relief

Generic: fexofenadine hcl
NDC Package

Package Facts

Identity

Package NDC 21130-405-30
Digits Only 2113040530
Product NDC 21130-405
Description

1 BOTTLE, PLASTIC in 1 BOX (21130-405-30) / 30 TABLET, COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Discontinued 2026-12-28
Brand iallergy relief
Generic fexofenadine hcl
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "db4f310d-a5a4-4896-8f44-193302785c5d", "openfda": {"upc": ["0321130763185"], "unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["1f6a97e3-f84a-4c89-8e8f-6e0d111fe500"], "manufacturer_name": ["Safeway, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (21130-405-30)  / 30 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "21130-405-30", "marketing_end_date": "20261228", "marketing_start_date": "20200228"}], "brand_name": "IAllergy Relief", "product_id": "21130-405_db4f310d-a5a4-4896-8f44-193302785c5d", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "21130-405", "generic_name": "Fexofenadine HCl", "labeler_name": "Safeway, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "IAllergy Relief", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA204507", "marketing_category": "ANDA", "marketing_end_date": "20261228", "marketing_start_date": "20200228"}