Package 58602-860-76

Brand: cetirizine hydrochloride

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 58602-860-76
Digits Only 5860286076
Product NDC 58602-860
Description

4 BLISTER PACK in 1 CARTON (58602-860-76) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2021-02-12
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": "99f8f81a-d083-48c1-a923-4ed0dfcd989f", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1011482"], "spl_set_id": ["c111f6f3-e190-447f-b4a4-e277af641483"], "manufacturer_name": ["Aurohealth LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 BLISTER PACK in 1 CARTON (58602-860-76)  / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK", "package_ndc": "58602-860-76", "marketing_start_date": "20210212"}], "brand_name": "Cetirizine Hydrochloride", "product_id": "58602-860_99f8f81a-d083-48c1-a923-4ed0dfcd989f", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "58602-860", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "Aurohealth LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cetirizine Hydrochloride", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA213557", "marketing_category": "ANDA", "marketing_start_date": "20210212", "listing_expiration_date": "20261231"}