Package 50090-5220-0

Brand: cetirizine hydrochloride

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-5220-0
Digits Only 5009052200
Product NDC 50090-5220
Product ID 50090-5220_65b3119c-c65e-41cc-b45b-aa615835a0b0
Description

1 BOTTLE in 1 CARTON (50090-5220-0) / 120 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2020-10-07
Brand cetirizine hydrochloride
Generic cetirizine hydrochloride
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "65b3119c-c65e-41cc-b45b-aa615835a0b0", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014673"], "spl_set_id": ["e626bd59-dd18-465c-b740-9d04eb48c28e"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (50090-5220-0)  / 120 mL in 1 BOTTLE", "package_ndc": "50090-5220-0", "marketing_start_date": "20201007"}], "brand_name": "Cetirizine Hydrochloride", "product_id": "50090-5220_65b3119c-c65e-41cc-b45b-aa615835a0b0", "dosage_form": "SOLUTION", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "50090-5220", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cetirizine Hydrochloride", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "1 mg/mL"}], "application_number": "ANDA076601", "marketing_category": "ANDA", "marketing_start_date": "20140501", "listing_expiration_date": "20261231"}