Package 51660-066-30

Brand: cetirizine hydrochloride

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51660-066-30
Digits Only 5166006630
Product NDC 51660-066
Description

1 BOTTLE in 1 CARTON (51660-066-30) / 30 TABLET, CHEWABLE in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2022-07-21
Brand cetirizine hydrochloride
Generic cetirizine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1ae46a4b-8176-44fc-bc57-ed9e62c02746", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014674"], "spl_set_id": ["97802669-b4bd-4807-b3c1-6c6f5a2b0c67"], "manufacturer_name": ["OHM LABORATORIES INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (51660-066-30)  / 30 TABLET, CHEWABLE in 1 BOTTLE", "package_ndc": "51660-066-30", "marketing_start_date": "20220721"}], "brand_name": "Cetirizine Hydrochloride", "product_id": "51660-066_1ae46a4b-8176-44fc-bc57-ed9e62c02746", "dosage_form": "TABLET, CHEWABLE", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "51660-066", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "OHM LABORATORIES INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cetirizine Hydrochloride", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA090142", "marketing_category": "ANDA", "marketing_start_date": "20220721", "listing_expiration_date": "20261231"}