Package 58602-823-39
Brand: cetirizine hydrochloride (allergy)
Generic: cetirizine hydrochloridePackage Facts
Identity
Package NDC
58602-823-39
Digits Only
5860282339
Product NDC
58602-823
Description
1 BOTTLE in 1 CARTON (58602-823-39) / 365 TABLET in 1 BOTTLE
Marketing
Marketing Status
Brand
cetirizine hydrochloride (allergy)
Generic
cetirizine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "bd9c2a41-9024-46a4-87c6-7d6f5f1fafbf", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["7d214cba-951d-464e-b37e-e83098944fe6"], "manufacturer_name": ["Aurohealth LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-823-39) / 365 TABLET in 1 BOTTLE", "package_ndc": "58602-823-39", "marketing_start_date": "20150805"}], "brand_name": "Cetirizine Hydrochloride (Allergy)", "product_id": "58602-823_bd9c2a41-9024-46a4-87c6-7d6f5f1fafbf", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "58602-823", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "Aurohealth LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cetirizine Hydrochloride (Allergy)", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA090760", "marketing_category": "ANDA", "marketing_start_date": "20150805", "listing_expiration_date": "20261231"}