Package 58602-862-76
Brand: cetirizine hydrochloride
Generic: cetirizine hydrochloridePackage Facts
Identity
Package NDC
58602-862-76
Digits Only
5860286276
Product NDC
58602-862
Description
4 BLISTER PACK in 1 CARTON (58602-862-76) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
Marketing
Marketing Status
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": "c6f65c7b-e626-4ef3-910d-03702cac03bf", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1011482"], "spl_set_id": ["d9ebebb5-736a-4019-8c1a-030148de9d02"], "manufacturer_name": ["Aurohealth LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 BLISTER PACK in 1 CARTON (58602-862-76) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK", "package_ndc": "58602-862-76", "marketing_start_date": "20210218"}], "brand_name": "Cetirizine Hydrochloride", "product_id": "58602-862_c6f65c7b-e626-4ef3-910d-03702cac03bf", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "58602-862", "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": "20210218", "listing_expiration_date": "20261231"}