Package 11822-0241-1

Brand: allergy relief

Generic: levocetirizine dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 11822-0241-1
Digits Only 1182202411
Product NDC 11822-0241
Description

1 BOTTLE in 1 CARTON (11822-0241-1) / 120 TABLET, FILM COATED in 1 BOTTLE

Marketing

Marketing Status
Discontinued 2026-11-30
Brand allergy relief
Generic levocetirizine dihydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b1f546c9-0566-4c68-bf78-e806284abd96", "openfda": {"unii": ["SOD6A38AGA"], "rxcui": ["855172"], "spl_set_id": ["c6f826a4-cb8d-4a9f-99cc-5041f65801ca"], "manufacturer_name": ["Rite Aid Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (11822-0241-1)  / 120 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "11822-0241-1", "marketing_end_date": "20261130", "marketing_start_date": "20201005"}], "brand_name": "allergy relief", "product_id": "11822-0241_b1f546c9-0566-4c68-bf78-e806284abd96", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "11822-0241", "generic_name": "levocetirizine dihydrochloride", "labeler_name": "Rite Aid Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "allergy relief", "active_ingredients": [{"name": "LEVOCETIRIZINE DIHYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA211983", "marketing_category": "ANDA", "marketing_end_date": "20261130", "marketing_start_date": "20201005"}