Package 21130-425-95
Brand: allergy relief
Generic: cetirizine hydrochloridePackage Facts
Identity
Package NDC
21130-425-95
Digits Only
2113042595
Product NDC
21130-425
Description
1 BOTTLE in 1 CARTON (21130-425-95) / 45 TABLET, FILM COATED in 1 BOTTLE
Marketing
Marketing Status
Brand
allergy relief
Generic
cetirizine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8b6eebd5-99d8-4acf-aec4-2b1c8d32ed4b", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["c5e74b2c-7871-4f28-a77d-0d674b9b8c5e"], "manufacturer_name": ["Safeway"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (21130-425-95) / 45 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "21130-425-95", "marketing_start_date": "20250911"}], "brand_name": "allergy relief", "product_id": "21130-425_8b6eebd5-99d8-4acf-aec4-2b1c8d32ed4b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "21130-425", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "Safeway", "product_type": "HUMAN OTC DRUG", "brand_name_base": "allergy relief", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078336", "marketing_category": "ANDA", "marketing_start_date": "20250911", "listing_expiration_date": "20261231"}