Package 21130-465-34

Brand: childrens allergy relief

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 21130-465-34
Digits Only 2113046534
Product NDC 21130-465
Description

1 BOTTLE in 1 CARTON (21130-465-34) / 240 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2024-07-31
Brand childrens 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": "81d6b4b4-2c46-4727-82fe-f7cedce89cc5", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014673"], "spl_set_id": ["5d3e4c52-b697-4b91-af28-124f74d937e5"], "manufacturer_name": ["Safeway"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (21130-465-34)  / 240 mL in 1 BOTTLE", "package_ndc": "21130-465-34", "marketing_start_date": "20240731"}], "brand_name": "childrens allergy relief", "product_id": "21130-465_81d6b4b4-2c46-4727-82fe-f7cedce89cc5", "dosage_form": "SOLUTION", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "21130-465", "generic_name": "cetirizine hydrochloride", "labeler_name": "Safeway", "product_type": "HUMAN OTC DRUG", "brand_name_base": "childrens allergy relief", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "5 mg/5mL"}], "application_number": "ANDA204226", "marketing_category": "ANDA", "marketing_start_date": "20240731", "listing_expiration_date": "20261231"}