Package 55319-939-30

Brand: cetirizine hydrochloride

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 55319-939-30
Digits Only 5531993930
Product NDC 55319-939
Description

30 TABLET in 1 BOTTLE (55319-939-30)

Marketing

Marketing Status
Marketed Since 2017-09-01
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": "65ed577d-07a6-40e5-bff5-26b9ec806f04", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["b326dacc-6123-47a7-9fde-6909db1d780b"], "manufacturer_name": ["FAMILY DOLLAR SERVICES, INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (55319-939-30)", "package_ndc": "55319-939-30", "marketing_start_date": "20170901"}, {"sample": false, "description": "14 TABLET in 1 BLISTER PACK (55319-939-54)", "package_ndc": "55319-939-54", "marketing_start_date": "20170901"}], "brand_name": "Cetirizine Hydrochloride", "product_id": "55319-939_65ed577d-07a6-40e5-bff5-26b9ec806f04", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "55319-939", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "FAMILY DOLLAR SERVICES, INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cetirizine Hydrochloride", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA077498", "marketing_category": "ANDA", "marketing_start_date": "20170901", "listing_expiration_date": "20261231"}