Package 50090-6168-3

Brand: cetirizine hydrochloride (allergy)

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-6168-3
Digits Only 5009061683
Product NDC 50090-6168
Description

90 TABLET in 1 BOTTLE (50090-6168-3)

Marketing

Marketing Status
Marketed Since 2023-08-02
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": "3f1dc2f9-4fb5-40a4-828f-205ce8ee8d16", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["158d3bcc-6a7f-4ee7-b181-be3fd6f94f8d"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-6168-1)", "package_ndc": "50090-6168-1", "marketing_start_date": "20221026"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-6168-3)", "package_ndc": "50090-6168-3", "marketing_start_date": "20230802"}], "brand_name": "Cetirizine Hydrochloride (Allergy)", "product_id": "50090-6168_3f1dc2f9-4fb5-40a4-828f-205ce8ee8d16", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "50090-6168", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "A-S Medication Solutions", "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": "20271231"}