Package 0363-9602-09

Brand: cetirizine hydrochloride (allergy)

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0363-9602-09
Digits Only 0363960209
Product NDC 0363-9602
Description

1 BOTTLE in 1 CARTON (0363-9602-09) / 30 TABLET in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2021-07-05
Brand cetirizine hydrochloride (allergy)
Generic cetirizine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7f752fde-e10a-4cbc-84bb-cd42849484c7", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["c0165b0e-d5e9-a028-e053-2a95a90ab431"], "manufacturer_name": ["WALGREEN CO."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-9602-09)  / 30 TABLET in 1 BOTTLE", "package_ndc": "0363-9602-09", "marketing_start_date": "20210705"}], "brand_name": "Cetirizine Hydrochloride (Allergy)", "product_id": "0363-9602_7f752fde-e10a-4cbc-84bb-cd42849484c7", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "0363-9602", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "WALGREEN CO.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cetirizine Hydrochloride (Allergy)", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA090760", "marketing_category": "ANDA", "marketing_start_date": "20210705", "listing_expiration_date": "20261231"}