Package 57483-250-01

Brand: crcle cetirizine hydrochloride

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 57483-250-01
Digits Only 5748325001
Product NDC 57483-250
Description

365 TABLET in 1 CONTAINER (57483-250-01)

Marketing

Marketing Status
Marketed Since 2023-04-28
Brand crcle 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": "b1644d9c-353b-44bf-b3f9-9bd8b83976f2", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["640583b6-379d-4ad3-b00c-383377c54eed"], "manufacturer_name": ["Innovus Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "365 TABLET in 1 CONTAINER (57483-250-01)", "package_ndc": "57483-250-01", "marketing_start_date": "20230428"}], "brand_name": "Crcle Cetirizine Hydrochloride", "product_id": "57483-250_b1644d9c-353b-44bf-b3f9-9bd8b83976f2", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "57483-250", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "Innovus Pharmaceuticals, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Crcle Cetirizine Hydrochloride", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA209274", "marketing_category": "ANDA", "marketing_start_date": "20210630", "listing_expiration_date": "20261231"}