Package 50090-6170-0

Brand: cetirizine hydrochloride (allergy)

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-6170-0
Digits Only 5009061700
Product NDC 50090-6170
Product ID 50090-6170_406f752b-552b-4c29-9ca8-4cbf82ad5ed6
Description

48 BOTTLE in 1 CASE (50090-6170-0) / 30 TABLET in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2022-10-13
Brand cetirizine hydrochloride (allergy)
Generic cetirizine hydrochloride
Sample Package No

Linked Drug Pages (1)

Cetirizine Hydrochloride (Allergy) ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "406f752b-552b-4c29-9ca8-4cbf82ad5ed6", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["42c9636f-07af-44a3-8d84-c11e1b57783a"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "48 BOTTLE in 1 CASE (50090-6170-0)  / 30 TABLET in 1 BOTTLE", "package_ndc": "50090-6170-0", "marketing_start_date": "20221013"}], "brand_name": "Cetirizine Hydrochloride (Allergy)", "product_id": "50090-6170_406f752b-552b-4c29-9ca8-4cbf82ad5ed6", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "50090-6170", "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": "20261231"}